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Volumn , Issue 13, 2001, Pages 2589-2594

The origin of chemical and configurational stability of chiral nonracemic tert-butyl aziridinecarboxylate anions

Author keywords

Aziridine; Configurational stability; Kinetic acidity; Nitrogen inversion; Quaternary amino esters

Indexed keywords

AZIRIDINE DERIVATIVE; PHENYLGLYCINE; TERT BUTYL AZIRIDINECARBOXYLATE; UNCLASSIFIED DRUG;

EID: 0034951174     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200107)2001:13<2589::AID-EJOC2589>3.0.CO;2-Y     Document Type: Article
Times cited : (35)

References (23)
  • 1
    • 0001318042 scopus 로고    scopus 로고
    • T. Satoh, Chem. Rev. 1996, 96, 3303-3325, and references therein.
    • (1996) Chem. Rev. , vol.96 , pp. 3303-3325
    • Satoh, T.1
  • 15
    • 0004674026 scopus 로고    scopus 로고
    • note
    • 1H NMR: The chemical shifts of the aziridinyl proton signals are typical for the (2R) or (2S) series.
  • 17
    • 0004656969 scopus 로고    scopus 로고
    • note
    • 1H NMR: The chemical shifts of the aziridinyl and tert-butyl ester proton signals are typical for the (2R) or (2S) series.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.