메뉴 건너뛰기




Volumn , Issue 20, 2004, Pages 4095-4105

Acetylenes in catalysis: Enantioselective additions to carbonyl groups and imines and applications beyond

Author keywords

Acetylenes; Catalysis; Enantioselectivity; Metal complexes

Indexed keywords

ACETIC ACID DERIVATIVE; ACETYLENE DERIVATIVE; ALCOHOL DERIVATIVE; ALDEHYDE; CARBONYL DERIVATIVE; ENAMINE; IMINE; KETONE; ORGANOMETALLIC COMPOUND; TITANIUM; ZINC;

EID: 8444224706     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200400246     Document Type: Short Survey
Times cited : (314)

References (156)
  • 1
    • 0242635970 scopus 로고    scopus 로고
    • For an excellent review on the asymmetric addition of alkynes to aldehydes and ketones, see: L. Pu, Tetrahedron 2003, 59, 9873-9886. For recent examples of the synthesis of chiral intermediates by enantioselective alkyne addition, see: J. A. Marshall, M. P. Borbeau, Org. Lett. 2003, 5, 3197-3199; and ref. cited therein.
    • (2003) Tetrahedron , vol.59 , pp. 9873-9886
    • Pu, L.1
  • 2
    • 0141521559 scopus 로고    scopus 로고
    • and ref. cited therein
    • For an excellent review on the asymmetric addition of alkynes to aldehydes and ketones, see: L. Pu, Tetrahedron 2003, 59, 9873-9886. For recent examples of the synthesis of chiral intermediates by enantioselective alkyne addition, see: J. A. Marshall, M. P. Borbeau, Org. Lett. 2003, 5, 3197-3199; and ref. cited therein.
    • (2003) Org. Lett. , vol.5 , pp. 3197-3199
    • Marshall, J.A.1    Borbeau, M.P.2
  • 4
    • 0001055858 scopus 로고    scopus 로고
    • (E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds.), Springer, Berlin, chapter 27
    • [3a] A. Yanagisawa, Comprehensive Asymmetric Catalysis (E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds.), Springer, Berlin, 1999, chapter 27, p. 965.
    • (1999) Comprehensive Asymmetric Catalysis , pp. 965
    • Yanagisawa, A.1
  • 5
    • 0001158063 scopus 로고    scopus 로고
    • (E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds.), Springer, Berlin, chapter 26
    • [3b] K. Soai, T. Shibata, Comprehensive Asymmetric Catalysis (E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds.), Springer, Berlin, 1999, chapter 26, p. 911.
    • (1999) Comprehensive Asymmetric Catalysis , pp. 911
    • Soai, K.1    Shibata, T.2
  • 11
    • 0011285592 scopus 로고    scopus 로고
    • D. Tzalis, P. Knochel, Angew. Chem. 1999, 111, 1547-1549; Angew. Chem. Int. Ed. 1999, 38, 1463-1465.
    • (1999) Angew. Chem. , vol.111 , pp. 1547-1549
    • Tzalis, D.1    Knochel, P.2
  • 12
    • 0033577829 scopus 로고    scopus 로고
    • D. Tzalis, P. Knochel, Angew. Chem. 1999, 111, 1547-1549; Angew. Chem. Int. Ed. 1999, 38, 1463-1465.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 1463-1465
  • 22
    • 0033105506 scopus 로고    scopus 로고
    • L. Tan, C.-Y. Chen, R. Tillyer, E. J. J. Grabowski, P. J. Reider, Angew. Chem. 1999, 111, 724-727; Angew. Chem. Int. Ed. 1999, 38, 711-713.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 711-713
  • 24
    • 0001956304 scopus 로고
    • R. Noyori, M. Kitamura, Angew. Chem. 1991, 103, 34-55; Angew. Chem. Int. Ed. Engl. 1991, 30, 49-69.
    • (1991) Angew. Chem. , vol.103 , pp. 34-55
    • Noyori, R.1    Kitamura, M.2
  • 25
    • 33745143561 scopus 로고
    • R. Noyori, M. Kitamura, Angew. Chem. 1991, 103, 34-55; Angew. Chem. Int. Ed. Engl. 1991, 30, 49-69.
    • (1991) Angew. Chem. Int. Ed. Engl. , vol.30 , pp. 49-69
  • 31
    • 84888981139 scopus 로고    scopus 로고
    • manuscript submitted
    • 2Zn alone is able to promote the addition of phenylacetylene to aldehydes and ketones. The transition state of the reaction was investigated by DFT calculations: P. G. Cozzi, J. Rudolph, C. Bolm, P. Nola-Orrby, C. Tomasini, manuscript submitted.
    • Cozzi, P.G.1    Rudolph, J.2    Bolm, C.3    Nola-Orrby, P.4    Tomasini, C.5
  • 33
    • 0034596803 scopus 로고    scopus 로고
    • C. Bolm, N. Hermanns, J. P. Hildebrand, K. Muñiz, Angew. Chem. 2000, 112, 3607-3609; Angew. Chem. Int. Ed. 2000, 39, 3465-3467.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3465-3467
  • 35
    • 0041806596 scopus 로고    scopus 로고
    • J. Rudolph, T. Rasmussen, C. Bolm, P.-O. Norrby, Angew. Chem. 2003, 115, 3110-3113; Angew. Chem. Int. Ed. 2003, 42, 3002-3005.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 3002-3005
  • 41
    • 0033557464 scopus 로고    scopus 로고
    • K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523; Angew. Chem. Int. Ed. 1999, 38, 497-501.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 497-501
  • 49
    • 0034675555 scopus 로고    scopus 로고
    • K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R. Angelaud, Angew. Chem. 2000, 112, 3676-3701, Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3532-3556
  • 57
    • 0346152682 scopus 로고    scopus 로고
    • Z. Xu, R. Wang, J. Xu, C.-S. Da, W.-J. Yan, C. Chen, Angew. Chem. 2003, 115, 5925-5927; Angew. Chem. Int. Ed. 2003, 42, 5747-5749.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5747-5749
  • 59
    • 84888976563 scopus 로고    scopus 로고
    • personal communication
    • M. Kozlowski, personal communication.
    • Kozlowski, M.1
  • 79
    • 0347131100 scopus 로고    scopus 로고
    • D. J. Ramón, M. Yus, Angew. Chem. Int. Ed. 2004, 116, 286-289; Angew. Chem. Int. Ed. 2004, 43, 284.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 284
  • 81
    • 0000946629 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (1999) Org. Lett. , vol.1 , pp. 1061-1063
    • Casolari, S.1    D'Adario, D.2    Tagliavini, E.3
  • 82
    • 0037933550 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (2002) Angew. Chem. , vol.114 , pp. 3849-13842
    • Waltz, K.M.1    Gavenonis, J.2    Walsh, P.J.3
  • 83
    • 0037020373 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 3697-3699
  • 84
    • 84888935944 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (2002) Angew. Chem. , vol.114 , pp. 1504-1508
    • Deng, H.1    Isler, M.P.2    Snapper, M.L.3    Hoveyda, A.H.4
  • 85
    • 0037087605 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1009-1012
  • 86
    • 0034596326 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (2000) J. Am. Chem. Soc. , vol.41 , pp. 7412-7413
    • Hamashima, Y.1    Kanai, M.2    Shibasaki, M.3
  • 87
    • 0032554099 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 445-446
    • Dosa, P.I.1    Fu, G.C.2
  • 88
    • 0032554843 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (1998) Tetrahedron , vol.54 , pp. 5651-5666
    • Ramón, D.J.1    Yus, M.2
  • 89
    • 0037130643 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10970-10971
    • Garcia, C.1    LaRochelle, L.K.2    Walsh, P.J.3
  • 90
    • 0037202209 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10970-10971
    • Dimauro, E.F.1    Kozlowski, M.C.2
  • 91
    • 0037414559 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 1103-1114
    • Ramón, D.1    Yus, M.2    Prieto, O.3
  • 92
    • 0043127350 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 9544-9545
    • Jeon, S.-J.1    Walsh, P.J.2
  • 93
    • 0142074832 scopus 로고    scopus 로고
    • For further methodologies on the addition of nucleophiles to ketones, see: [60a] S. Casolari, D. D'Adario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063. [60b] K. M. Waltz, J. Gavenonis, P. J. Walsh, Angew. Chem. 2002, 114, 3849-3842; Angew. Chem. Int. Ed. 2002, 41, 3697-3699. [60c] H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 2002, 114, 1504-1508; Angew. Chem. Int. Ed. 2002, 41, 1009-1012. [60d] Y. Hamashima, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2000, 41, 7412-7413. [60e] P. I. Dosa, G. C. Fu, J. Am. Chem. Soc. 1998, 120, 445-446. [60f] D. J. Ramón, M. Yus, Tetrahedron 1998, 54, 5651-5666. [60g] C. Garcia, L. K. LaRochelle, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60h] E. F. DiMauro, M. C. Kozlowski, J. Am. Chem. Soc. 2002, 124, 10970-10971. [60i] D. Ramón, M. Yus, O. Prieto, Tetrahedron: Asymmetry 2003, 14, 1103-1114. [60j] S.-J. Jeon, P. J. Walsh, J. Am. Chem. Soc. 2003, 125, 9544-9545. [60k] C. Garcia, P. J. Walsh, Org. Lett. 2003, 5, 3641-3644.
    • (2003) Org. Lett. , vol.5 , pp. 3641-3644
    • Garcia, C.1    Walsh, P.J.2
  • 95
    • 0242307576 scopus 로고    scopus 로고
    • P. G. Cozzi, Angew. Chem. 2003, 115, 3001-3004; Angew. Chem. Int. Ed. 2003, 42, 2895-2898.
    • (2003) Angew. Chem. , vol.115 , pp. 3001-3004
    • Cozzi, P.G.1
  • 96
    • 0038711344 scopus 로고    scopus 로고
    • P. G. Cozzi, Angew. Chem. 2003, 115, 3001-3004; Angew. Chem. Int. Ed. 2003, 42, 2895-2898.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 2895-2898
  • 104
    • 0242291909 scopus 로고    scopus 로고
    • G. Lu, X. Li, X. Jia, W. L. Chan, A. S. C. Chan, Angew. Chem. 2003, 115, 5211-5212; Angew. Chem. Int. Ed. 2003, 42, 5057-5058.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5057-5058
  • 114
    • 0000862669 scopus 로고    scopus 로고
    • and ref. cited therein
    • S. Kobayashi, H. Ishitani, Chem. Rev. 1999, 99, 1069-1094, and ref. cited therein.
    • (1999) Chem. Rev. , vol.99 , pp. 1069-1094
    • Kobayashi, S.1    Ishitani, H.2
  • 116
    • 0030794772 scopus 로고    scopus 로고
    • S. Berger, F. Langer, C. Lutz, P. Knochel, T. A. Mobley, C. Kishan Reddy, Angew. Chem. 1997, 109, 1605-1607; Angew. Chem. Int. Ed. Engl. 1997, 36, 1496-1498; for theoretical investigations on mixed Zinc reagents, see ref. [23].
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1496-1498
  • 118
    • 0037099190 scopus 로고    scopus 로고
    • [79a] C. Koradin, K. Polborn, P. Knochel, Angew. Chem. 2002, 114, 2651-2654; Angew. Chem. Int. Ed. 2002, 41, 2535-2538.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2535-2538
  • 120
    • 0346243940 scopus 로고    scopus 로고
    • [79b] N. Gommermann, C. Koradin, K. Polborn, P. Knochel, Angew. Chem. 2003, 115, 5941-5944; Angew. Chem. Int. Ed. 2003, 42, 5763-5766.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5763-5766
  • 121
    • 8444230338 scopus 로고    scopus 로고
    • B. Jiang, Y.-G. Si, Angew. Chem. 2004, 116, 218-220; Angew. Chem. Int. Ed. 2004, 43, 216-218.
    • (2004) Angew. Chem. , vol.116 , pp. 218-220
    • Jiang, B.1    Si, Y.-G.2
  • 122
    • 33745716283 scopus 로고    scopus 로고
    • B. Jiang, Y.-G. Si, Angew. Chem. 2004, 116, 218-220; Angew. Chem. Int. Ed. 2004, 43, 216-218.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 216-218
  • 124
    • 0043031390 scopus 로고    scopus 로고
    • B. M. Trost, Z. T. Ball, T. Jöge, Angew. Chem. 2003, 115, 3537-3540; Angew. Chem. Int. Ed. 2003, 42, 3415-3418.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 3415-3418
  • 128
    • 0000096835 scopus 로고    scopus 로고
    • [84a] H. C. Kolb, M. G. Finn, K. B. Sharpless, Angew. Chem. 2001, 113, 2056-2075; Angew. Chem. Int. Ed. 2001, 40, 2004-2021.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 2004-2021
  • 131
    • 0037087516 scopus 로고    scopus 로고
    • W. G. Lewis, L. G. Green, F. Grynszpan, Z. Radic, P. R. Carlier, P. Taylor, M. G. Finn, K. B. Sharpless, Angew. Chem. 2002, 114, 1095-1099; Angew. Chem. Int. Ed. 2002, 41, 1053-1057.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1053-1057
  • 134
    • 0037099395 scopus 로고    scopus 로고
    • [86b] V. V. Rostovtsev, L. G. Green, V. V. Fokin, K. B. Sharpless, Angew. Chem. 2002, 114, 2708-2711; Angew. Chem. Int. Ed. 2002, 41, 2596-2599.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2596-2599
  • 146
  • 148
    • 8444246196 scopus 로고    scopus 로고
    • S. P. Shahi, K. Koide, Angew. Chem. 2004, 116, 2579-2581; Angew. Chem. Int. Ed. 2004, 43, 2525-2527.
    • (2004) Angew. Chem. , vol.116 , pp. 2579-2581
    • Shahi, S.P.1    Koide, K.2
  • 149
    • 2942596792 scopus 로고    scopus 로고
    • S. P. Shahi, K. Koide, Angew. Chem. 2004, 116, 2579-2581; Angew. Chem. Int. Ed. 2004, 43, 2525-2527.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 2525-2527


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.