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Volumn 21, Issue 13-14, 2010, Pages 1635-1648

Doubly diastereoselective conjugate addition of enantiopure lithium amides to enantiopure N-enoyl oxazolidin-2-ones: A mechanistic probe

Author keywords

[No Author keywords available]

Indexed keywords

3 [3' [N BENZYL N (ALPHA METHYLBENZYL) AMINO] BUTANOYL] 4 BENZYLOXAZOLIDIN 2 ONE; AMIDE; LITHIUM DERIVATIVE; N 1' HYDROXY 3' PHENYLPROPAN 2' YL 3 [N' [2'' N'' (TERT BUTOXYCARBONYL)AMINO 3'' PHENYLPROPANOYL]AMINO] 3 PHENYLPROPANAMIDE; N(3) (3' AMINO 3' PHENYLPROPANOYL) 4 BENZYLOXAZOLIDIN 2 ONE; N(3) (3' PHENYLPROPENOYL) 4 BENZYLOXAZOLIDIN 2 ONE; N(3) (3' PHENYLPROPENOYL) 4 PHENYLOXAZOLIDIN 2 ONE; N(3) (4' METHYLPENT 2 'ENOYL) 4 BENZYLOXAZOLIDIN 2 ONE; N(3) [1' TRIETHYLSILYLOXY 3' [N BENZYL N (ALPHA METHYLBENZYL)AMINO] 3' PHENYLPROP 2' ENYL] 4 BENZYLOXAZOLIDIN 2 ONE; N(3) [3' (N,N DIBENZYLAMINO) 3' PHENYLPROPANOYL] 4 BENZYLOXAZOLIDIN 2 ONE; N(3) [3' (N,N DIBENZYLAMINO) 3' PHENYLPROPANOYL] 4 PHENYLOXAZOLIDIN 2 ONE; N(3) [3' (N,N DIBENZYLAMINO) 4' METHYLPENTANOYL] 4 BENZYLOXAZOLIDIN 2 ONE; N(3) [3' (N,N DIBENZYLAMINO)BUTANOYL] 4 BENZYLOXAZOLIDIN 2 ONE; N(3) [3' (N,N DIBENZYLAMINO)BUTANOYL] 4 PHENYLOXAZOLIDIN 2 ONE; N(3) [3' [N BENZYL N (ALPHA METHYLBENZYL)AMINO] 3' PHENYLPROPANOYL] 4 BENZYLOXAZOLIDIN 2 ONE; N(3) [3' [N BENZYL N (ALPHA METHYLBENZYL)AMINO] 3' PHENYLPROPANOYL] 4 PHENYLOXAZOLIDIN 2 ONE; N(3) [3' [N BENZYL N (ALPHA METHYLBENZYL)AMINO] 4' METHYLPENTANOYL] 4 BENZYLOXAZOLIDIN 2 ONE; N(3) [3' [N BENZYL N (ALPHA METHYLBENZYL)AMINO] BUTANOYL] 4 PHENYLOXAZOLIDIN 2 ONE; N(3) [3' [N BENZYL N (ALPHA METHYLBENZYL)AMINO]BUTANOYL] 4 BENZYLOXAZOLIDIN ONE; N(3) [3' [N BENZYL N (ALPHA METHYLBENZYL)AMINO]BUTANOYL] 4 PHENYLOXAZOLIDIN 2 ONE; N(3) [3' [N' [2'' N'' (TERT BUTOXYCARBONYL) AMINO 3'' PHENYLPROPANOYL]AMINO] 3' PHENYLPROPANOYL] 4 BENZYLOXAZOLIDIN 2 ONE; N(3) BUT 2' ENOYL 4 BENZYLOXAZOLIDIN 2 ONE; N(3) BUT 2' ENOYL 4 PHENYLOXAZOLIDIN 2 ONE; N,N DIBENZYL 3 (N,N DIBENZYLAMINO) 4 METHYLPENTANAMIDE; OXAZOLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77956264668     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2010.03.033     Document Type: Article
Times cited : (21)

References (57)
  • 4
    • 0001743772 scopus 로고
    • For other examples, specifically detailing the use of chiral auxiliaries, see: T. Mukaiyama, and N. Iwasawa Chem. Lett. 1981 913
    • (1981) Chem. Lett. , pp. 913
    • Mukaiyama, T.1    Iwasawa, N.2
  • 15
    • 0001486864 scopus 로고
    • For NMR investigations of the conformations adopted by oxazolidinones in asymmetric reactions, see: S. Castellino, and W.J. Dwight J. Am. Chem. Soc. 115 1993 2986
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 2986
    • Castellino, S.1    Dwight, W.J.2
  • 22
    • 0038486072 scopus 로고    scopus 로고
    • For examples of amide addition to achiral oxazolidinone systems with chiral catalysts see: K. Li, and K.K. Hii Chem. Commun. 2003 1132
    • (2003) Chem. Commun. , pp. 1132
    • Li, K.1    Hii, K.K.2
  • 48
    • 77956266698 scopus 로고    scopus 로고
    • note
    • 1H NMR chiral shift analysis using (R)-O-acetylmandelic acid.
  • 53


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.