메뉴 건너뛰기




Volumn 28, Issue 2, 2009, Pages 448-464

Insertion of isocyanides, isothiocyanates, and carbon monoxide into the pd-c bond of cyclopalladated complexes containing primary arylalkylamines of biological and pharmaceutical significance. synthesis of lactams and cyclic amidinium salts related to the isoquinoline, benzo[g]isoquinoline, and β-carboline nuclei

Author keywords

[No Author keywords available]

Indexed keywords

ACETONITRILE; AMIDES; AMINO ACIDS; CARBON MONOXIDE; CRYSTAL STRUCTURE; CYANIDES; DERIVATIVES; DIFFRACTION; ESTERIFICATION; ESTERS; ORGANOMETALLICS; PALLADIUM; SALTS; STEREOCHEMISTRY; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL); TOLUENE; X RAY DIFFRACTION;

EID: 61849182496     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om800951k     Document Type: Article
Times cited : (85)

References (202)
  • 46
    • 34548735913 scopus 로고    scopus 로고
    • Albert, J.; D?ndrea, L.; Granell, J.; Zafrilla, J.; Font-Bardia, M.; Solans, X. J. Organomet. Chem. 2007, 692, 4895.
    • Albert, J.; D?ndrea, L.; Granell, J.; Zafrilla, J.; Font-Bardia, M.; Solans, X. J. Organomet. Chem. 2007, 692, 4895.
  • 56
    • 0003601534 scopus 로고    scopus 로고
    • 12th ed, Merck: Rahway, NJ
    • The Merck Index, 12th ed.; Merck: Rahway, NJ, 1996, p 1244.
    • (1996) The Merck Index , pp. 1244
  • 57
    • 0003601534 scopus 로고    scopus 로고
    • 12th ed, Merck: Rahway, NJ
    • The Merck Index, 12th ed.; Merck: Rahway, NJ, 1996; p 1251.
    • (1996) The Merck Index , pp. 1251
  • 58
    • 0003601534 scopus 로고    scopus 로고
    • 12th ed, Merck: Rahway, NJ
    • The Merck Index, 12th ed.; Merck: Rahway, NJ, 1996, p 1669.
    • (1996) The Merck Index , pp. 1669
  • 59
    • 61849085108 scopus 로고    scopus 로고
    • Numbers assigned to the synthesized compounds include the letter of their parent complexes. Thus, compounds la-5a are derivatives of cyclopalladated naphthylalanine methyl ester A, compounds lb-5b are synthesized from complex B, compounds 3c-5c are synthesized from C, and compounds 3d-5d are synthesized from D
    • Numbers assigned to the synthesized compounds include the letter of their parent complexes. Thus, compounds la-5a are derivatives of cyclopalladated naphthylalanine methyl ester (A), compounds lb-5b are synthesized from complex B, compounds 3c-5c are synthesized from C, and compounds 3d-5d are synthesized from D.
  • 61
    • 0014438541 scopus 로고    scopus 로고
    • Doskotch, R. W.; Sch?fí, P. L.; Beal, J. L. Tetrahedron 1969, 25, 469.
    • Doskotch, R. W.; Sch?fí, P. L.; Beal, J. L. Tetrahedron 1969, 25, 469.
  • 65
    • 0042657819 scopus 로고    scopus 로고
    • Chang, Y.-C; Chang, F.-R.; Khalil, A. T.; Hsieh, P.-W.; Wu, Y.-C. Z Naturforsch., C: J. Biosci. 2003, 58, 521.
    • Chang, Y.-C; Chang, F.-R.; Khalil, A. T.; Hsieh, P.-W.; Wu, Y.-C. Z Naturforsch., C: J. Biosci. 2003, 58, 521.
  • 77
    • 0024566078 scopus 로고    scopus 로고
    • Clark, R. D.; Jahangir, J. Org. Chem. 1989, 54, 1174.
    • Clark, R. D.; Jahangir, J. Org. Chem. 1989, 54, 1174.
  • 100
    • 0000554392 scopus 로고    scopus 로고
    • Clark, R. D.; Jahangir, J. Org. Chem. 1987, 52, 5378.
    • Clark, R. D.; Jahangir, J. Org. Chem. 1987, 52, 5378.
  • 106
    • 0035858621 scopus 로고    scopus 로고
    • Bois-Choussy, M.; De Paolis, M.; Zhu, J. Tetrahedron Lett. 2001, 42, 3427. Beccalli, E. M.; Broggini, G.; Marchesinia, A.; Rossia, E. Tetrahedron 2002, 58, 6673.
    • Bois-Choussy, M.; De Paolis, M.; Zhu, J. Tetrahedron Lett. 2001, 42, 3427. Beccalli, E. M.; Broggini, G.; Marchesinia, A.; Rossia, E. Tetrahedron 2002, 58, 6673.
  • 139
    • 0037011767 scopus 로고    scopus 로고
    • Vicente, J.; Areas, A.; Bautista, D.; Ramirez de. Arellano, M. C. J. Organomet. Chem. 2002, 663, 164.
    • Vicente, J.; Areas, A.; Bautista, D.; Ramirez de. Arellano, M. C. J. Organomet. Chem. 2002, 663, 164.
  • 156
    • 61849127673 scopus 로고    scopus 로고
    • Sato, F.; Noguchi, J.; Sato, M. J. Organomet. Chem. 1976, 118, 117. (b) Cámpora, J.; Gutiérrez, E.; Monge, A.; Palma, P.; Poveda, M. L.; Ruiz, C; Carmona, E. Organometallics 1994, 13, 1728.
    • (a) Sato, F.; Noguchi, J.; Sato, M. J. Organomet. Chem. 1976, 118, 117. (b) Cámpora, J.; Gutiérrez, E.; Monge, A.; Palma, P.; Poveda, M. L.; Ruiz, C; Carmona, E. Organometallics 1994, 13, 1728.
  • 183
    • 37049084917 scopus 로고    scopus 로고
    • Vicente, J.; Saura-Llamas, 1.; Palin, M. G.; Jones, P. G. J. Chem. Soc. Dalton Trans. 1995, 2535.
    • Vicente, J.; Saura-Llamas, 1.; Palin, M. G.; Jones, P. G. J. Chem. Soc. Dalton Trans. 1995, 2535.
  • 196
    • 61849138199 scopus 로고    scopus 로고
    • Sheldrick, G. M. SHELX-97; University of Göttingen, Göttingen, Germany, 1997.
    • Sheldrick, G. M. SHELX-97; University of Göttingen, Göttingen, Germany, 1997.
  • 197
    • 84944438568 scopus 로고    scopus 로고
    • Flack, H, D. Acta Crystallogr., Sect. A 1983, 39, 876.
    • Flack, H, D. Acta Crystallogr., Sect. A 1983, 39, 876.
  • 198
    • 61849128708 scopus 로고    scopus 로고
    • Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Montgomery, J. A, Jr, Vreven, T, Kudin, K. N, Burant, J. C; Millam, J. M, Iyengar, S. S, Tomasi, J, Barone, V, Mennucci, B, Cossi, M, Scalmani, G, Rega, N, Petersson, G. A, Nakatsuji, H, Hada, M, Ehara, M, Toyota, K, Fukuda, R, Hasegawa, J, Ishida, M, Nakajima, T, Honda, Y, Kitao, 0, Nakai, H, Klene, M, Li, X, Knox, J. E, Hratchian, H. P, Cross, J. B, Bakken, V, Adamo, C; Jaramillo, J, Gomperts, R, Stratmann, R. E, Yazyev, O, Austin, A. J, Cammi, R, Pomelli, C; Ochterski, J. W, Ayala, P. Y, Morokuma, K, Voth, G. A, Salvador, P, Dannenberg, J. J, Zakrzewski, V. G, Dapprich, S, Daniels, A. D, Strain, M. C; Farkas, O, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Ortiz, J. V, Cui, Q, Baboul, A. G, Clifford, S, Cioslowski, J, Stefanov, B. B, Liu, G, Liashenko, A, Piskorz, P, Komaromi, I, Martin, R. L, Fox, D. J, Keith, T
    • Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A., Jr.; Vreven, T.; Kudin, K. N.; Burant, J. C; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, 0.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Bakken, V.; Adamo, C; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M,; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez, C; Pople, J. A. Gaussian 03, revision C.02; Gaussian, Inc., Wallingford, CT, 2004.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.