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Volumn 67, Issue 21, 2002, Pages 7361-7364

Total synthesis of anhydrolycorinone utilizing sequential intramolecular Diels-Alder reactions of a 1,3,4-oxadiazole

Author keywords

[No Author keywords available]

Indexed keywords

INTRAMOLECULAR REACTIONS;

EID: 0037131146     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo020437k     Document Type: Article
Times cited : (83)

References (81)
  • 6
    • 33845373668 scopus 로고
    • Boger, D. L.; Coleman, R. S. J. Org. Chem. 1986, 51, 3250. Boger, D. L.; Coleman, R. S. J. Am. Chem. Soc. 1987, 109, 2717. Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415. Boger, D. L.; Zhang, M. J. Am. Chem. Soc. 1991, 113, 4230. Boger, D. L.; Schaum, R. P.; Garbaccio, R. M. J. Org. Chem. 1998, 63, 6329. For reviews of heterocyclic azadiene Diels-Alder reactions, see: Boger, D. L. Tetrahedron 1983, 39, 2869. Boger, D. L. Chem. Rev. 1986, 86, 781. Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149. Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987.
    • (1986) J. Org. Chem. , vol.51 , pp. 3250
    • Boger, D.L.1    Coleman, R.S.2
  • 7
    • 33845283430 scopus 로고
    • Boger, D. L.; Coleman, R. S. J. Org. Chem. 1986, 51, 3250. Boger, D. L.; Coleman, R. S. J. Am. Chem. Soc. 1987, 109, 2717. Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415. Boger, D. L.; Zhang, M. J. Am. Chem. Soc. 1991, 113, 4230. Boger, D. L.; Schaum, R. P.; Garbaccio, R. M. J. Org. Chem. 1998, 63, 6329. For reviews of heterocyclic azadiene Diels-Alder reactions, see: Boger, D. L. Tetrahedron 1983, 39, 2869. Boger, D. L. Chem. Rev. 1986, 86, 781. Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149. Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 2717
    • Boger, D.L.1    Coleman, R.S.2
  • 8
    • 33845280522 scopus 로고
    • Boger, D. L.; Coleman, R. S. J. Org. Chem. 1986, 51, 3250. Boger, D. L.; Coleman, R. S. J. Am. Chem. Soc. 1987, 109, 2717. Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415. Boger, D. L.; Zhang, M. J. Am. Chem. Soc. 1991, 113, 4230. Boger, D. L.; Schaum, R. P.; Garbaccio, R. M. J. Org. Chem. 1998, 63, 6329. For reviews of heterocyclic azadiene Diels-Alder reactions, see: Boger, D. L. Tetrahedron 1983, 39, 2869. Boger, D. L. Chem. Rev. 1986, 86, 781. Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149. Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987.
    • (1988) J. Org. Chem. , vol.53 , pp. 1415
    • Boger, D.L.1    Sakya, S.M.2
  • 9
    • 0025871436 scopus 로고
    • Boger, D. L.; Coleman, R. S. J. Org. Chem. 1986, 51, 3250. Boger, D. L.; Coleman, R. S. J. Am. Chem. Soc. 1987, 109, 2717. Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415. Boger, D. L.; Zhang, M. J. Am. Chem. Soc. 1991, 113, 4230. Boger, D. L.; Schaum, R. P.; Garbaccio, R. M. J. Org. Chem. 1998, 63, 6329. For reviews of heterocyclic azadiene Diels-Alder reactions, see: Boger, D. L. Tetrahedron 1983, 39, 2869. Boger, D. L. Chem. Rev. 1986, 86, 781. Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149. Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4230
    • Boger, D.L.1    Zhang, M.2
  • 10
    • 0001688605 scopus 로고    scopus 로고
    • Boger, D. L.; Coleman, R. S. J. Org. Chem. 1986, 51, 3250. Boger, D. L.; Coleman, R. S. J. Am. Chem. Soc. 1987, 109, 2717. Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415. Boger, D. L.; Zhang, M. J. Am. Chem. Soc. 1991, 113, 4230. Boger, D. L.; Schaum, R. P.; Garbaccio, R. M. J. Org. Chem. 1998, 63, 6329. For reviews of heterocyclic azadiene Diels-Alder reactions, see: Boger, D. L. Tetrahedron 1983, 39, 2869. Boger, D. L. Chem. Rev. 1986, 86, 781. Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149. Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987.
    • (1998) J. Org. Chem. , vol.63 , pp. 6329
    • Boger, D.L.1    Schaum, R.P.2    Garbaccio, R.M.3
  • 11
    • 45449097286 scopus 로고
    • Boger, D. L.; Coleman, R. S. J. Org. Chem. 1986, 51, 3250. Boger, D. L.; Coleman, R. S. J. Am. Chem. Soc. 1987, 109, 2717. Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415. Boger, D. L.; Zhang, M. J. Am. Chem. Soc. 1991, 113, 4230. Boger, D. L.; Schaum, R. P.; Garbaccio, R. M. J. Org. Chem. 1998, 63, 6329. For reviews of heterocyclic azadiene Diels-Alder reactions, see: Boger, D. L. Tetrahedron 1983, 39, 2869. Boger, D. L. Chem. Rev. 1986, 86, 781. Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149. Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987.
    • (1983) Tetrahedron , vol.39 , pp. 2869
    • Boger, D.L.1
  • 12
    • 33845376451 scopus 로고
    • Boger, D. L.; Coleman, R. S. J. Org. Chem. 1986, 51, 3250. Boger, D. L.; Coleman, R. S. J. Am. Chem. Soc. 1987, 109, 2717. Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415. Boger, D. L.; Zhang, M. J. Am. Chem. Soc. 1991, 113, 4230. Boger, D. L.; Schaum, R. P.; Garbaccio, R. M. J. Org. Chem. 1998, 63, 6329. For reviews of heterocyclic azadiene Diels-Alder reactions, see: Boger, D. L. Tetrahedron 1983, 39, 2869. Boger, D. L. Chem. Rev. 1986, 86, 781. Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149. Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987.
    • (1986) Chem. Rev. , vol.86 , pp. 781
    • Boger, D.L.1
  • 13
    • 0000229010 scopus 로고    scopus 로고
    • Boger, D. L.; Coleman, R. S. J. Org. Chem. 1986, 51, 3250. Boger, D. L.; Coleman, R. S. J. Am. Chem. Soc. 1987, 109, 2717. Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415. Boger, D. L.; Zhang, M. J. Am. Chem. Soc. 1991, 113, 4230. Boger, D. L.; Schaum, R. P.; Garbaccio, R. M. J. Org. Chem. 1998, 63, 6329. For reviews of heterocyclic azadiene Diels-Alder reactions, see: Boger, D. L. Tetrahedron 1983, 39, 2869. Boger, D. L. Chem. Rev. 1986, 86, 781. Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149. Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987.
    • (1996) Chemtracts: Org. Chem. , vol.9 , pp. 149
    • Boger, D.L.1
  • 14
    • 0003719612 scopus 로고
    • Academic: San Diego
    • Boger, D. L.; Coleman, R. S. J. Org. Chem. 1986, 51, 3250. Boger, D. L.; Coleman, R. S. J. Am. Chem. Soc. 1987, 109, 2717. Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415. Boger, D. L.; Zhang, M. J. Am. Chem. Soc. 1991, 113, 4230. Boger, D. L.; Schaum, R. P.; Garbaccio, R. M. J. Org. Chem. 1998, 63, 6329. For reviews of heterocyclic azadiene Diels-Alder reactions, see: Boger, D. L. Tetrahedron 1983, 39, 2869. Boger, D. L. Chem. Rev. 1986, 86, 781. Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149. Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987.
    • (1987) Hetero Diels-Alder Methodology in Organic Synthesis
    • Boger, D.L.1    Weinreb, S.M.2
  • 15
    • 0023635676 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 5895
    • Hayakawa, K.1    Yasukouchi, T.2    Kanematsu, K.3
  • 16
    • 0028844190 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1995) J. Org. Chem. , vol.60 , pp. 6318
    • González, C.1    Pére, D.2    Guitián, E.3    Castedo, L.4
  • 17
    • 0030008275 scopus 로고    scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1996) J. Org. Chem. , vol.61 , pp. 1650
    • Pérez, D.1    Burés, G.2    Guitián, E.3    Castedo, L.4
  • 18
    • 0027225265 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1993) Synthesis , pp. 579
    • Grotjahn, D.B.1    Vollhardt, K.P.C.2
  • 19
    • 0000893946 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1962) J. Org. Chem. , vol.27 , pp. 142
    • Benington, F.1    Morin, R.D.2
  • 20
    • 0015984592 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1974) J. Med. Chem. , vol.17 , pp. 167
    • Olson, D.R.1    Wheeler, W.J.2    Wells, J.N.3
  • 21
    • 0031436173 scopus 로고    scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1997) J. Org. Chem. , vol.62 , pp. 9305
    • Bunnell, A.E.1    Flippin, L.A.2    Liu, Y.3
  • 22
    • 37049126992 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1974) J. Chem. Soc., Perkin Trans. 1 , pp. 1523
    • Carruthers, W.1    Evans, N.2
  • 23
    • 0001229543 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1974) Tetrahedron Lett. , vol.15 , pp. 1179
    • Onaka, T.1    Kanda, Y.2    Natsume, M.3
  • 24
    • 2142778374 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 5807
    • St. Black, D.C.1    Keller, P.A.2    Kumar, N.3
  • 25
    • 0025827238 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 3859
    • Grigg, R.1    Teasdale, A.2    Sridharan, V.3
  • 26
    • 0027531203 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1993) Tetrahedron , vol.49 , pp. 151
    • St. Black, D.C.1    Keller, P.A.2    Kumar, N.3
  • 27
    • 0000886231 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1993) Heterocycles , vol.36 , pp. 2597
    • Sakamoto, T.1    Yasuhara, A.2    Kondo, Y.3    Yamanaka, H.4
  • 28
    • 0032871544 scopus 로고    scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1999) Synthesis , pp. 1300
    • Harrowven, D.C.1    Lai, D.2    Lucas, M.C.3
  • 29
    • 0033522818 scopus 로고    scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 4347
    • Miki, Y.1    Shirokoshi, H.2    Matsushita, K.3
  • 30
    • 0002889982 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1972) Tetrahedron Lett. , vol.13 , pp. 5031
    • Hara, H.1    Hoshino, O.2    Umezawa, B.3
  • 31
    • 37049096211 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1978) J. Chem. Soc., Chem. Commun. , pp. 766
    • Iida, H.1    Yuasa, Y.2    Kibayashi, C.3
  • 32
    • 0017863106 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1978) J. Med. Chem. , vol.21 , pp. 199
    • Zee-Cheng, R.K.-Y.1    Yan, S.-J.2    Cheng, C.C.3
  • 33
    • 0025959190 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 65
    • Lauk, U.1    Dürst, D.2    Fischer, W.3
  • 34
    • 0030446696 scopus 로고    scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1996) J. Org. Chem. , vol.61 , pp. 9168
    • Xiong, Y.1    Moore, H.W.2
  • 35
    • 0032377834 scopus 로고    scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1998) Chem. Lett. , pp. 155
    • Tsuge, O.1    Hatta, T.2    Tsuchiyama, H.3
  • 36
    • 0006687577 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1987) J. Chem. Res., Synop. , pp. 167
    • Prabhakar, S.1    Lobo, A.M.2    Marques, M.M.3
  • 37
    • 0025237306 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1523
    • Siddiqui, M.A.1    Snieckus, V.2
  • 38
    • 0028024370 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.;
    • (1994) J. Org. Chem. , vol.59 , pp. 3497
    • Parnes, J.S.1    Carter, D.S.2    Kurz, L.J.3    Flippin, L.A.4
  • 39
    • 0001332710 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1994) Heterocycles , vol.38 , pp. 1717
    • Iwao, M.1    Takehara, H.2    Obata, S.3    Watanabe, M.4
  • 40
    • 37049067873 scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1995) J. Chem. Soc., Chem. Commun. , pp. 2551
    • Banwell, M.G.1    Bissett, B.D.2    Busato, S.3    Cowden, C.J.4    Hockless, D.C.R.5    Holman, J.W.6    Read, R.W.7    Wu, A.W.8
  • 41
    • 0030063927 scopus 로고    scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (1996) J. Org. Chem. , vol.61 , pp. 1004
    • Hutchings, R.H.1    Meyers, A.I.2
  • 42
    • 0034685857 scopus 로고    scopus 로고
    • N-Alkylation, Diels-Alder reaction: Hayakawa, K.; Yasukouchi, T.; Kanematsu, K. Tetrahedron Lett. 1987, 28, 5895. González, C.; Pére, D.; Guitián, E.; Castedo, L. J. Org. Chem. 1995, 60, 6318. Pérez, D.; Burés, G.; Guitián, E.; Castedo, L. J. Org. Chem. 1996, 61, 1650. Metal-catalyzed [2 + 2 + 2] cycloaddition: Grotjahn, D. B.; Vollhardt, K. P. C. Synthesis 1993, 579. N-Alkylation, electrophilic aromatic substitution: Benington, F.; Morin, R. D. J. Org. Chem. 1962, 27, 142. Olson, D. R.; Wheeler, W. J.; Wells, J. N. J. Med. Chem. 1974, 17, 167. Bunnell, A. E.; Flippin, L. A.; Liu, Y. J. Org. Chem. 1997, 62, 9305. N-Alkylation, metal-catalyzed ring closure: Carruthers, W.; Evans, N. J. Chem. Soc., Perkin Trans. 1 1974, 1523. Onaka, T.; Kanda, Y.; Natsume, M. Tetrahedron Lett. 1974, 15, 1179. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron Lett. 1989, 30, 5807. Grigg, R.; Teasdale, A.; Sridharan, V. Tetrahedron Lett. 1991, 32, 3859. Black, D. St. C.; Keller, P. A.; Kumar, N. Tetrahedron 1993, 49, 151. Sakamoto, T.; Yasuhara, A.; Kondo, Y.; Yamanaka, H. Heterocycles 1993, 36, 2597. Harrowven, D. C.; Lai, D.; Lucas, M. C. Synthesis 1999, 1300. Miki, Y.; Shirokoshi, H.; Matsushita, K. Tetrahedron Lett. 1999, 40, 4347. N-Alkylation, radical ring closure: Hara, H.; Hoshino, O.; Umezawa, B. Tetrahedron Lett. 1972, 13, 5031. Iida, H.; Yuasa, Y.; Kibayashi, C. J. Chem. Soc., Chem. Commun. 1978, 766. Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem. 1978, 21, 199. Lauk, U.; Dürst, D.; Fischer, W. Tetrahedron Lett. 1991, 32, 65. Xiong, Y.; Moore, H. W. J. Org. Chem. 1996, 61, 9168. Tsuge, O.; Hatta, T.; Tsuchiyama, H. Chem. Lett. 1998, 155. Biaryl formation, N-alkylation: Prabhakar, S.; Lobo, A. M.; Marques, M. M. J. Chem. Res., Synop. 1987, 167. Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett. 1990, 31, 1523. Parnes, J. S.; Carter, D. S.; Kurz, L. J.; Flippin, L. A. J. Org. Chem. 1994, 59, 3497. Iwao, M.; Takehara, H.; Obata, S.; Watanabe, M. Heterocycles 1994, 38, 1717. Banwell, M. G.; Bissett, B. D.; Busato, S.; Cowden, C. J.; Hockless, D. C. R.; Holman, J. W.; Read, R. W.; Wu, A. W. J. Chem. Soc., Chem. Commun. 1995, 2551. Hutchings, R. H.; Meyers, A. I. J. Org. Chem. 1996, 61, 1004. Stark, L. M.; Lin, X.-F.; Flippin, L. A. J. Org. Chem. 2000, 65, 3227.
    • (2000) J. Org. Chem. , vol.65 , pp. 3227
    • Stark, L.M.1    Lin, X.-F.2    Flippin, L.A.3
  • 45
    • 4243699055 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1987) Khim. Geterotsikl. Soedin. , pp. 562
    • Vasiliev, N.V.1    Lyashenko, Y.E.2    Kolomiets, A.F.3    Sokolskii, G.A.4
  • 46
    • 0003946822 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1990) Khim. Geterotsikl. Soedin. , pp. 95
    • Vasiliev, N.V.1    Lyashenko, Y.E.2    Galakhov, M.V.3    Kolomiets, A.F.4    Gontar, A.F.5    Sokolskii, G.A.6
  • 47
    • 0001664134 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1993) J. Fluorine Chem. , vol.65 , pp. 227
    • Vasilíev, N.V.1    Lyashenko, Y.E.2    Patalakha, A.E.3    Sokolskii, G.A.4
  • 48
    • 0001473172 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 3231
    • Thalhammer, F.1    Wallfahrer, U.2    Sauer, J.3
  • 49
    • 0028211192 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1994) Pharmazie , vol.49 , pp. 102
    • Seitz, G.1    Gerninghaus, C.H.2
  • 50
    • 0002965961 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1988) Chem.-Ztg. , vol.112 , pp. 80
    • Seitz, G.1    Wassmuth, H.2
  • 51
    • 0033755004 scopus 로고    scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (2000) Eur. J. Org. Chem. , pp. 3363
    • Warrener, R.N.1
  • 52
    • 0035857266 scopus 로고    scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (2001) Tetrahedron , vol.57 , pp. 571
    • Warrener, R.N.1    Margetic, D.2    Foley, P.J.3    Butler, D.N.4    Winling, A.5    Beales, K.A.6    Russell, R.A.7
  • 53
    • 0029100698 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 6141
    • Warrener, R.N.1    Wang, S.2    Maksimovic, L.3    Tepperman, P.M.4    Butler, D.N.5
  • 54
    • 0029070731 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 5275
    • Warrener, R.N.1    Elsey, G.M.2    Russell, R.A.3    Tiekink, E.R.T.4
  • 55
    • 37049071793 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1994) J. Chem. Soc., Chem. Commun. , pp. 1831
    • Warrener, R.N.1    Maksimovic, L.2    Butler, D.N.3
  • 56
    • 0026083324 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 1889
    • Warrener, R.N.1    Butler, D.N.2    Liao, W.Y.3    Pitt, I.G.4    Russell, R.A.5
  • 57
    • 0026084965 scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 1885
    • Warrener, R.N.1    Groundwater, P.2    Pitt, I.G.3    Butler, D.N.4    Russell, R.A.5
  • 58
    • 0001987071 scopus 로고    scopus 로고
    • Vasiliev, N. V.; Lyashenko, Y. E.; Kolomiets, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1987, 562. Vasiliev, N. V.; Lyashenko, Y. E.; Galakhov, M. V.; Kolomiets, A. F.; Gontar, A. F.; Sokolskii, G. A. Khim. Geterotsikl. Soedin. 1990, 95. Vasilíev, N. V.; Lyashenko, Y. E.; Patalakha, A. E.; Sokolskii, G. A. J. Fluorine Chem. 1993, 65, 227. Thalhammer, F.; Wallfahrer, U.; Sauer, J. Tetrahedron Lett. 1988, 29, 3231. Seitz, G.; Gerninghaus, C. H. Pharmazie 1994, 49, 102. Seitz, G.; Wassmuth, H. Chem.-Ztg. 1988, 112, 80. Review: Warrener, R. N. Eur. J. Org. Chem. 2000, 3363. Warrener, R. N.; Margetic, D.; Foley, P. J.; Butler, D. N.; Winling, A.; Beales, K. A.; Russell, R. A. Tetrahedron 2001, 57, 571. Warrener, R. N.; Wang, S.; Maksimovic, L.; Tepperman, P. M.; Butler, D. N. Tetrahedron Lett. 1995, 36, 6141. Warrener, R. N.; Elsey, G. M.; Russell, R. A.; Tiekink, E. R. T. Tetrahedron Lett. 1995, 36, 5275. Warrener, R. N.; Maksimovic, L.; Butler, D. N. J. Chem. Soc., Chem. Commun. 1994, 1831. Warrener, R. N.; Butler, D. N.; Liao, W. Y.; Pitt, I. G.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1889. Warrener, R. N.; Groundwater, P.; Pitt, I. G.; Butler, D. N.; Russell, R. A. Tetrahedron Lett. 1991, 32, 1885. Warrener, R. N.; Margetic, D.; Tiekink, E. R. T.; Russell, R. A. Synlett 1997, 196.
    • (1997) Synlett , pp. 196
    • Warrener, R.N.1    Margetic, D.2    Tiekink, E.R.T.3    Russell, R.A.4
  • 60
    • 0003719612 scopus 로고
    • Academic: San Diego
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987; pp 301-310. For examples, see: Grigg, R.; Jackson, J. L. J. Chem. Soc. C 1970, 552. Ansell, M. F.; Caton, M. P. L.; North, P. C. Tetrahedron Lett. 1981, 22, 1727. Jacobi, P. A.; Walker, D. G.; Odeh, I. M. A. J. Org. Chem. 1981, 46, 5. Liotta, D.; Saindane, M.; Ott, W. Tetrahedron Lett. 1983, 24, 2473. Jacobi, P. A.; Craig, T. A.; Walker, D. G.; Arrick, B. A.; Frechette, R. F. J. Am. Chem. Soc. 1984, 106, 5585. Selnick, H. G.; Brookes, L. M. Tetrahedron Lett. 1989, 30, 6607. Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384. Yadav, J. S.; Valluri, M.; Rao, A. V. R. Tetrahedron Lett. 1994, 35, 3609. Rao, A. V. R.; Yadav, J. S.; Valluri, M. Tetrahedron Lett. 1994, 35, 3613.
    • (1987) Hetero Diels-Alder Methodology in Organic Synthesis , pp. 301-310
    • Boger, D.L.1    Weinreb, S.M.2
  • 61
    • 37049123141 scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987; pp 301-310. For examples, see: Grigg, R.; Jackson, J. L. J. Chem. Soc. C 1970, 552. Ansell, M. F.; Caton, M. P. L.; North, P. C. Tetrahedron Lett. 1981, 22, 1727. Jacobi, P. A.; Walker, D. G.; Odeh, I. M. A. J. Org. Chem. 1981, 46, 5. Liotta, D.; Saindane, M.; Ott, W. Tetrahedron Lett. 1983, 24, 2473. Jacobi, P. A.; Craig, T. A.; Walker, D. G.; Arrick, B. A.; Frechette, R. F. J. Am. Chem. Soc. 1984, 106, 5585. Selnick, H. G.; Brookes, L. M. Tetrahedron Lett. 1989, 30, 6607. Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384. Yadav, J. S.; Valluri, M.; Rao, A. V. R. Tetrahedron Lett. 1994, 35, 3609. Rao, A. V. R.; Yadav, J. S.; Valluri, M. Tetrahedron Lett. 1994, 35, 3613.
    • (1970) J. Chem. Soc. C , pp. 552
    • Grigg, R.1    Jackson, J.L.2
  • 62
    • 0019473681 scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987; pp 301-310. For examples, see: Grigg, R.; Jackson, J. L. J. Chem. Soc. C 1970, 552. Ansell, M. F.; Caton, M. P. L.; North, P. C. Tetrahedron Lett. 1981, 22, 1727. Jacobi, P. A.; Walker, D. G.; Odeh, I. M. A. J. Org. Chem. 1981, 46, 5. Liotta, D.; Saindane, M.; Ott, W. Tetrahedron Lett. 1983, 24, 2473. Jacobi, P. A.; Craig, T. A.; Walker, D. G.; Arrick, B. A.; Frechette, R. F. J. Am. Chem. Soc. 1984, 106, 5585. Selnick, H. G.; Brookes, L. M. Tetrahedron Lett. 1989, 30, 6607. Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384. Yadav, J. S.; Valluri, M.; Rao, A. V. R. Tetrahedron Lett. 1994, 35, 3609. Rao, A. V. R.; Yadav, J. S.; Valluri, M. Tetrahedron Lett. 1994, 35, 3613.
    • (1981) Tetrahedron Lett. , vol.22 , pp. 1727
    • Ansell, M.F.1    Caton, M.P.L.2    North, P.C.3
  • 63
    • 2142831429 scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987; pp 301-310. For examples, see: Grigg, R.; Jackson, J. L. J. Chem. Soc. C 1970, 552. Ansell, M. F.; Caton, M. P. L.; North, P. C. Tetrahedron Lett. 1981, 22, 1727. Jacobi, P. A.; Walker, D. G.; Odeh, I. M. A. J. Org. Chem. 1981, 46, 5. Liotta, D.; Saindane, M.; Ott, W. Tetrahedron Lett. 1983, 24, 2473. Jacobi, P. A.; Craig, T. A.; Walker, D. G.; Arrick, B. A.; Frechette, R. F. J. Am. Chem. Soc. 1984, 106, 5585. Selnick, H. G.; Brookes, L. M. Tetrahedron Lett. 1989, 30, 6607. Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384. Yadav, J. S.; Valluri, M.; Rao, A. V. R. Tetrahedron Lett. 1994, 35, 3609. Rao, A. V. R.; Yadav, J. S.; Valluri, M. Tetrahedron Lett. 1994, 35, 3613.
    • (1981) J. Org. Chem. , vol.46 , pp. 5
    • Jacobi, P.A.1    Walker, D.G.2    Odeh, I.M.A.3
  • 64
    • 0000625668 scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987; pp 301-310. For examples, see: Grigg, R.; Jackson, J. L. J. Chem. Soc. C 1970, 552. Ansell, M. F.; Caton, M. P. L.; North, P. C. Tetrahedron Lett. 1981, 22, 1727. Jacobi, P. A.; Walker, D. G.; Odeh, I. M. A. J. Org. Chem. 1981, 46, 5. Liotta, D.; Saindane, M.; Ott, W. Tetrahedron Lett. 1983, 24, 2473. Jacobi, P. A.; Craig, T. A.; Walker, D. G.; Arrick, B. A.; Frechette, R. F. J. Am. Chem. Soc. 1984, 106, 5585. Selnick, H. G.; Brookes, L. M. Tetrahedron Lett. 1989, 30, 6607. Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384. Yadav, J. S.; Valluri, M.; Rao, A. V. R. Tetrahedron Lett. 1994, 35, 3609. Rao, A. V. R.; Yadav, J. S.; Valluri, M. Tetrahedron Lett. 1994, 35, 3613.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 2473
    • Liotta, D.1    Saindane, M.2    Ott, W.3
  • 65
    • 0021205323 scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987; pp 301-310. For examples, see: Grigg, R.; Jackson, J. L. J. Chem. Soc. C 1970, 552. Ansell, M. F.; Caton, M. P. L.; North, P. C. Tetrahedron Lett. 1981, 22, 1727. Jacobi, P. A.; Walker, D. G.; Odeh, I. M. A. J. Org. Chem. 1981, 46, 5. Liotta, D.; Saindane, M.; Ott, W. Tetrahedron Lett. 1983, 24, 2473. Jacobi, P. A.; Craig, T. A.; Walker, D. G.; Arrick, B. A.; Frechette, R. F. J. Am. Chem. Soc. 1984, 106, 5585. Selnick, H. G.; Brookes, L. M. Tetrahedron Lett. 1989, 30, 6607. Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384. Yadav, J. S.; Valluri, M.; Rao, A. V. R. Tetrahedron Lett. 1994, 35, 3609. Rao, A. V. R.; Yadav, J. S.; Valluri, M. Tetrahedron Lett. 1994, 35, 3613.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 5585
    • Jacobi, P.A.1    Craig, T.A.2    Walker, D.G.3    Arrick, B.A.4    Frechette, R.F.5
  • 66
    • 0024803099 scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987; pp 301-310. For examples, see: Grigg, R.; Jackson, J. L. J. Chem. Soc. C 1970, 552. Ansell, M. F.; Caton, M. P. L.; North, P. C. Tetrahedron Lett. 1981, 22, 1727. Jacobi, P. A.; Walker, D. G.; Odeh, I. M. A. J. Org. Chem. 1981, 46, 5. Liotta, D.; Saindane, M.; Ott, W. Tetrahedron Lett. 1983, 24, 2473. Jacobi, P. A.; Craig, T. A.; Walker, D. G.; Arrick, B. A.; Frechette, R. F. J. Am. Chem. Soc. 1984, 106, 5585. Selnick, H. G.; Brookes, L. M. Tetrahedron Lett. 1989, 30, 6607. Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384. Yadav, J. S.; Valluri, M.; Rao, A. V. R. Tetrahedron Lett. 1994, 35, 3609. Rao, A. V. R.; Yadav, J. S.; Valluri, M. Tetrahedron Lett. 1994, 35, 3613.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 6607
    • Selnick, H.G.1    Brookes, L.M.2
  • 67
    • 0001421951 scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987; pp 301-310. For examples, see: Grigg, R.; Jackson, J. L. J. Chem. Soc. C 1970, 552. Ansell, M. F.; Caton, M. P. L.; North, P. C. Tetrahedron Lett. 1981, 22, 1727. Jacobi, P. A.; Walker, D. G.; Odeh, I. M. A. J. Org. Chem. 1981, 46, 5. Liotta, D.; Saindane, M.; Ott, W. Tetrahedron Lett. 1983, 24, 2473. Jacobi, P. A.; Craig, T. A.; Walker, D. G.; Arrick, B. A.; Frechette, R. F. J. Am. Chem. Soc. 1984, 106, 5585. Selnick, H. G.; Brookes, L. M. Tetrahedron Lett. 1989, 30, 6607. Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384. Yadav, J. S.; Valluri, M.; Rao, A. V. R. Tetrahedron Lett. 1994, 35, 3609. Rao, A. V. R.; Yadav, J. S.; Valluri, M. Tetrahedron Lett. 1994, 35, 3613.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 5384
    • Jacobi, P.A.1    Blum, C.A.2    DeSimone, R.W.3    Udodong, U.E.S.4
  • 68
    • 0028276503 scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987; pp 301-310. For examples, see: Grigg, R.; Jackson, J. L. J. Chem. Soc. C 1970, 552. Ansell, M. F.; Caton, M. P. L.; North, P. C. Tetrahedron Lett. 1981, 22, 1727. Jacobi, P. A.; Walker, D. G.; Odeh, I. M. A. J. Org. Chem. 1981, 46, 5. Liotta, D.; Saindane, M.; Ott, W. Tetrahedron Lett. 1983, 24, 2473. Jacobi, P. A.; Craig, T. A.; Walker, D. G.; Arrick, B. A.; Frechette, R. F. J. Am. Chem. Soc. 1984, 106, 5585. Selnick, H. G.; Brookes, L. M. Tetrahedron Lett. 1989, 30, 6607. Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384. Yadav, J. S.; Valluri, M.; Rao, A. V. R. Tetrahedron Lett. 1994, 35, 3609. Rao, A. V. R.; Yadav, J. S.; Valluri, M. Tetrahedron Lett. 1994, 35, 3613.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 3609
    • Yadav, J.S.1    Valluri, M.2    Rao, A.V.R.3
  • 69
    • 0028263735 scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic: San Diego, 1987; pp 301-310. For examples, see: Grigg, R.; Jackson, J. L. J. Chem. Soc. C 1970, 552. Ansell, M. F.; Caton, M. P. L.; North, P. C. Tetrahedron Lett. 1981, 22, 1727. Jacobi, P. A.; Walker, D. G.; Odeh, I. M. A. J. Org. Chem. 1981, 46, 5. Liotta, D.; Saindane, M.; Ott, W. Tetrahedron Lett. 1983, 24, 2473. Jacobi, P. A.; Craig, T. A.; Walker, D. G.; Arrick, B. A.; Frechette, R. F. J. Am. Chem. Soc. 1984, 106, 5585. Selnick, H. G.; Brookes, L. M. Tetrahedron Lett. 1989, 30, 6607. Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384. Yadav, J. S.; Valluri, M.; Rao, A. V. R. Tetrahedron Lett. 1994, 35, 3609. Rao, A. V. R.; Yadav, J. S.; Valluri, M. Tetrahedron Lett. 1994, 35, 3613.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 3613
    • Rao, A.V.R.1    Yadav, J.S.2    Valluri, M.3
  • 70
    • 0000569625 scopus 로고
    • Aside from oxazoles, few cycloaddition approaches to substituted furans have been described: Gotthardt, H.; Huisgen, R.; Bayer, H. O. J. Am. Chem. Soc. 1970, 92, 4340. Wilson, W. S.; Warrener, R. N. J. Chem. Soc., Chem. Commun. 1972, 211. Ho, M. S.; Wong, H. N. C. J. Chem. Soc., Chem. Commun. 1989, 1238.
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 4340
    • Gotthardt, H.1    Huisgen, R.2    Bayer, H.O.3
  • 71
    • 37049131031 scopus 로고
    • Aside from oxazoles, few cycloaddition approaches to substituted furans have been described: Gotthardt, H.; Huisgen, R.; Bayer, H. O. J. Am. Chem. Soc. 1970, 92, 4340. Wilson, W. S.; Warrener, R. N. J. Chem. Soc., Chem. Commun. 1972, 211. Ho, M. S.; Wong, H. N. C. J. Chem. Soc., Chem. Commun. 1989, 1238.
    • (1972) J. Chem. Soc., Chem. Commun. , pp. 211
    • Wilson, W.S.1    Warrener, R.N.2
  • 72
    • 37049070478 scopus 로고
    • Aside from oxazoles, few cycloaddition approaches to substituted furans have been described: Gotthardt, H.; Huisgen, R.; Bayer, H. O. J. Am. Chem. Soc. 1970, 92, 4340. Wilson, W. S.; Warrener, R. N. J. Chem. Soc., Chem. Commun. 1972, 211. Ho, M. S.; Wong, H. N. C. J. Chem. Soc., Chem. Commun. 1989, 1238.
    • (1989) J. Chem. Soc., Chem. Commun. , pp. 1238
    • Ho, M.S.1    Wong, H.N.C.2
  • 73
    • 2142849128 scopus 로고    scopus 로고
    • Katritzky, A. R., Rees, C.W., Scriven, E. F. V., Eds.; Elsevier: New York
    • Heaney, H.; Ahn, J. S. In Comprehensive Heterocylic Chemistry, 2nd ed.; Katritzky, A. R., Rees, C. W., Scriven, E. F. V., Eds.; Elsevier: New York, 1996; Vol. 2, pp 328-335. For examples, see: Parker, K. A.; Adamchuk, M. R. Tetrahedron Lett. 1978, 18, 1689. Sternbach, D. D.; Rossana, D. M. J. Am. Chem. Soc. 1982, 104, 5853. Van Royen, L. A.; Mijngheer, R.; De Clercq, P. J. Tetrahedron Lett. 1983, 24, 3145. Sternbach, D. D.; Rossana, D. M.; Onan, K. D. J. Org. Chem. 1984, 49, 3427. Trost, B. M.; Lautens, M.; Hung, M.-H.; Carmichael, C. S. J. Am. Chem. Soc. 1984, 106, 7641. Jung, M. E.; Street, L. J. J. Am. Chem. Soc. 1984, 106, 8327.
    • (1996) Comprehensive Heterocylic Chemistry, 2nd ed. , vol.2 , pp. 328-335
    • Heaney, H.1    Ahn, J.S.2
  • 74
    • 0000235146 scopus 로고
    • Heaney, H.; Ahn, J. S. In Comprehensive Heterocylic Chemistry, 2nd ed.; Katritzky, A. R., Rees, C. W., Scriven, E. F. V., Eds.; Elsevier: New York, 1996; Vol. 2, pp 328-335. For examples, see: Parker, K. A.; Adamchuk, M. R. Tetrahedron Lett. 1978, 18, 1689. Sternbach, D. D.; Rossana, D. M. J. Am. Chem. Soc. 1982, 104, 5853. Van Royen, L. A.; Mijngheer, R.; De Clercq, P. J. Tetrahedron Lett. 1983, 24, 3145. Sternbach, D. D.; Rossana, D. M.; Onan, K. D. J. Org. Chem. 1984, 49, 3427. Trost, B. M.; Lautens, M.; Hung, M.-H.; Carmichael, C. S. J. Am. Chem. Soc. 1984, 106, 7641. Jung, M. E.; Street, L. J. J. Am. Chem. Soc. 1984, 106, 8327.
    • (1978) Tetrahedron Lett. , vol.18 , pp. 1689
    • Parker, K.A.1    Adamchuk, M.R.2
  • 75
    • 0001742391 scopus 로고
    • Heaney, H.; Ahn, J. S. In Comprehensive Heterocylic Chemistry, 2nd ed.; Katritzky, A. R., Rees, C. W., Scriven, E. F. V., Eds.; Elsevier: New York, 1996; Vol. 2, pp 328-335. For examples, see: Parker, K. A.; Adamchuk, M. R. Tetrahedron Lett. 1978, 18, 1689. Sternbach, D. D.; Rossana, D. M. J. Am. Chem. Soc. 1982, 104, 5853. Van Royen, L. A.; Mijngheer, R.; De Clercq, P. J. Tetrahedron Lett. 1983, 24, 3145. Sternbach, D. D.; Rossana, D. M.; Onan, K. D. J. Org. Chem. 1984, 49, 3427. Trost, B. M.; Lautens, M.; Hung, M.-H.; Carmichael, C. S. J. Am. Chem. Soc. 1984, 106, 7641. Jung, M. E.; Street, L. J. J. Am. Chem. Soc. 1984, 106, 8327.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 5853
    • Sternbach, D.D.1    Rossana, D.M.2
  • 76
    • 0001340207 scopus 로고
    • Heaney, H.; Ahn, J. S. In Comprehensive Heterocylic Chemistry, 2nd ed.; Katritzky, A. R., Rees, C. W., Scriven, E. F. V., Eds.; Elsevier: New York, 1996; Vol. 2, pp 328-335. For examples, see: Parker, K. A.; Adamchuk, M. R. Tetrahedron Lett. 1978, 18, 1689. Sternbach, D. D.; Rossana, D. M. J. Am. Chem. Soc. 1982, 104, 5853. Van Royen, L. A.; Mijngheer, R.; De Clercq, P. J. Tetrahedron Lett. 1983, 24, 3145. Sternbach, D. D.; Rossana, D. M.; Onan, K. D. J. Org. Chem. 1984, 49, 3427. Trost, B. M.; Lautens, M.; Hung, M.-H.; Carmichael, C. S. J. Am. Chem. Soc. 1984, 106, 7641. Jung, M. E.; Street, L. J. J. Am. Chem. Soc. 1984, 106, 8327.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 3145
    • Van Royen, L.A.1    Mijngheer, R.2    De Clercq, P.J.3
  • 77
    • 0001549912 scopus 로고
    • Heaney, H.; Ahn, J. S. In Comprehensive Heterocylic Chemistry, 2nd ed.; Katritzky, A. R., Rees, C. W., Scriven, E. F. V., Eds.; Elsevier: New York, 1996; Vol. 2, pp 328-335. For examples, see: Parker, K. A.; Adamchuk, M. R. Tetrahedron Lett. 1978, 18, 1689. Sternbach, D. D.; Rossana, D. M. J. Am. Chem. Soc. 1982, 104, 5853. Van Royen, L. A.; Mijngheer, R.; De Clercq, P. J. Tetrahedron Lett. 1983, 24, 3145. Sternbach, D. D.; Rossana, D. M.; Onan, K. D. J. Org. Chem. 1984, 49, 3427. Trost, B. M.; Lautens, M.; Hung, M.-H.; Carmichael, C. S. J. Am. Chem. Soc. 1984, 106, 7641. Jung, M. E.; Street, L. J. J. Am. Chem. Soc. 1984, 106, 8327.
    • (1984) J. Org. Chem. , vol.49 , pp. 3427
    • Sternbach, D.D.1    Rossana, D.M.2    Onan, K.D.3
  • 78
    • 0000005129 scopus 로고
    • Heaney, H.; Ahn, J. S. In Comprehensive Heterocylic Chemistry, 2nd ed.; Katritzky, A. R., Rees, C. W., Scriven, E. F. V., Eds.; Elsevier: New York, 1996; Vol. 2, pp 328-335. For examples, see: Parker, K. A.; Adamchuk, M. R. Tetrahedron Lett. 1978, 18, 1689. Sternbach, D. D.; Rossana, D. M. J. Am. Chem. Soc. 1982, 104, 5853. Van Royen, L. A.; Mijngheer, R.; De Clercq, P. J. Tetrahedron Lett. 1983, 24, 3145. Sternbach, D. D.; Rossana, D. M.; Onan, K. D. J. Org. Chem. 1984, 49, 3427. Trost, B. M.; Lautens, M.; Hung, M.-H.; Carmichael, C. S. J. Am. Chem. Soc. 1984, 106, 7641. Jung, M. E.; Street, L. J. J. Am. Chem. Soc. 1984, 106, 8327.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 7641
    • Trost, B.M.1    Lautens, M.2    Hung, M.-H.3    Carmichael, C.S.4
  • 79
    • 33645171082 scopus 로고
    • Heaney, H.; Ahn, J. S. In Comprehensive Heterocylic Chemistry, 2nd ed.; Katritzky, A. R., Rees, C. W., Scriven, E. F. V., Eds.; Elsevier: New York, 1996; Vol. 2, pp 328-335. For examples, see: Parker, K. A.; Adamchuk, M. R. Tetrahedron Lett. 1978, 18, 1689. Sternbach, D. D.; Rossana, D. M. J. Am. Chem. Soc. 1982, 104, 5853. Van Royen, L. A.; Mijngheer, R.; De Clercq, P. J. Tetrahedron Lett. 1983, 24, 3145. Sternbach, D. D.; Rossana, D. M.; Onan, K. D. J. Org. Chem. 1984, 49, 3427. Trost, B. M.; Lautens, M.; Hung, M.-H.; Carmichael, C. S. J. Am. Chem. Soc. 1984, 106, 7641. Jung, M. E.; Street, L. J. J. Am. Chem. Soc. 1984, 106, 8327.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 8327
    • Jung, M.E.1    Street, L.J.2


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