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Volumn 14, Issue 21, 2003, Pages 3353-3358

Synthesis of a conformationally restricted analog of pregabalin by stereoselective alkylation of a chiral pyrrolidin-2-one

Author keywords

[No Author keywords available]

Indexed keywords

3 BENZYLOXYMETHYL 1 (TERT BUTOXYCARBONYL) 4 (2' METHYLPROP 1' YL)PYRROLIDINE; 4 BENZYLOXYMETHYL 3 (2'' METHYLPROP 1'' YL) 1 (1' PHENYLETHYL)PYRROLIDIN 2 ONE; 4 BENZYLOXYMETHYL 3 (2'' METHYLPROP 1'' YL) 1 (1' PHENYLETHYL)PYRROLIDINE; 4 BENZYLOXYMETHYLPYRROLIDIN 2 ONE; BENZYL DERIVATIVE; CARBONYL DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; KETONE DERIVATIVE; NITROGEN; PREGABALIN; PYRROLIDINE CARBOXYLIC ACID; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0142196046     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(03)00599-8     Document Type: Article
Times cited : (21)

References (26)
  • 19
    • 0024802559 scopus 로고
    • The alkylation of γ-lactams was generally carried out by first protecting the nitrogen atom with a carbamate. See, for example: (a) Baldwin, J. E.; Miranda, T.; Moloney, M. Tetrahedron 1989, 45, 7459-7468; (b) Hagen, T. J. Synlett 1990, 63-66; (c) Ezquerra, J.; Pedregal, C.; Rubio, A.; Yruretagoyena, B.; Escribano, A.; Sanchez-Ferrando F. Tetrahedron 1993, 49, 8665-8678; (d) Maldaner, A. O.; Pilli, R. A. Tetrahedron 1999, 55, 13321-13332.
    • (1989) Tetrahedron , vol.45 , pp. 7459-7468
    • Baldwin, J.E.1    Miranda, T.2    Moloney, M.3
  • 20
    • 85062280348 scopus 로고
    • The alkylation of γ-lactams was generally carried out by first protecting the nitrogen atom with a carbamate. See, for example: (a) Baldwin, J. E.; Miranda, T.; Moloney, M. Tetrahedron 1989, 45, 7459-7468; (b) Hagen, T. J. Synlett 1990, 63-66; (c) Ezquerra, J.; Pedregal, C.; Rubio, A.; Yruretagoyena, B.; Escribano, A.; Sanchez-Ferrando F. Tetrahedron 1993, 49, 8665-8678; (d) Maldaner, A. O.; Pilli, R. A. Tetrahedron 1999, 55, 13321-13332.
    • (1990) Synlett , pp. 63-66
    • Hagen, T.J.1
  • 21
    • 0027301896 scopus 로고
    • The alkylation of γ-lactams was generally carried out by first protecting the nitrogen atom with a carbamate. See, for example: (a) Baldwin, J. E.; Miranda, T.; Moloney, M. Tetrahedron 1989, 45, 7459-7468; (b) Hagen, T. J. Synlett 1990, 63-66; (c) Ezquerra, J.; Pedregal, C.; Rubio, A.; Yruretagoyena, B.; Escribano, A.; Sanchez-Ferrando F. Tetrahedron 1993, 49, 8665-8678; (d) Maldaner, A. O.; Pilli, R. A. Tetrahedron 1999, 55, 13321-13332.
    • (1993) Tetrahedron , vol.49 , pp. 8665-8678
    • Ezquerra, J.1    Pedregal, C.2    Rubio, A.3    Yruretagoyena, B.4    Escribano, A.5    Sanchez-Ferrando, F.6
  • 22
    • 0033585017 scopus 로고    scopus 로고
    • The alkylation of γ-lactams was generally carried out by first protecting the nitrogen atom with a carbamate. See, for example: (a) Baldwin, J. E.; Miranda, T.; Moloney, M. Tetrahedron 1989, 45, 7459-7468; (b) Hagen, T. J. Synlett 1990, 63-66; (c) Ezquerra, J.; Pedregal, C.; Rubio, A.; Yruretagoyena, B.; Escribano, A.; Sanchez-Ferrando F. Tetrahedron 1993, 49, 8665-8678; (d) Maldaner, A. O.; Pilli, R. A. Tetrahedron 1999, 55, 13321-13332.
    • (1999) Tetrahedron , vol.55 , pp. 13321-13332
    • Maldaner, A.O.1    Pilli, R.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.