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Volumn 50, Issue 28, 2009, Pages 4188-4190

Application of the addition of triorganozincates to N-(tert-butanesulfinyl)imines to the enantioselective synthesis of α-amino acids

Author keywords

Amino acid; Diastereoselective addition; Organozincate; Oxidative cleavage; Sulfinylimine

Indexed keywords

ALPHA AMINO ACID; AMINE; ESTER DERIVATIVE; IMINE; N (TERT BUTANESULFINYL)IMINE DERIVATIVE; TRIORGANOZINCATE DERIVATIVE; UNCLASSIFIED DRUG; ZINC DERIVATIVE;

EID: 66049128418     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.05.008     Document Type: Article
Times cited : (23)

References (43)
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  • 38
    • 66049157759 scopus 로고    scopus 로고
    • note
    • The removal of the sulfinyl group and the benzoylation of the obtained primary amines were carried out following the procedures previously described by us (see Ref. 7b).
  • 40
    • 66049127505 scopus 로고    scopus 로고
    • note
    • The ee's of the free amines were determined after benzoylation and analysis of the obtained benzamides 3 by HPLC using a ChiralCel OD-H column (see Ref. 7b). The enantiomeric ratios of the free primary amines were equal to the diastereomeric ratios of the corresponding sulfinamides 2.
  • 41
    • 0000231880 scopus 로고
    • Oxidative cleavage of the vinyl group:
    • Oxidative cleavage of the vinyl group:. Laschat S., and Kunz H. J. Org. Chem. 56 (1991) 5883-5889
    • (1991) J. Org. Chem. , vol.56 , pp. 5883-5889
    • Laschat, S.1    Kunz, H.2
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    • note
    • 3.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.