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Journal of Molecular Structure: THEOCHEM

Volumn 540, Issue 1-3, 2001, Pages 271-283

An exploratory ab initio study of the full conformational space of N-acetyl-L-cysteine-N-methylamide

(7) Zamora, M A a Baldoni, H A a Bombasaro, J A a Mak, M L b Perczel, A c,d Farkas, O c,e Enriz, R D a

a UNIVERSIDAD NACIONAL DE SAN LUIS (Argentina)

b UNIVERSITY OF TORONTO (Canada)

c EÖTVÖS LORÁND UNIVERSITY (Hungary)

d UNIVERSITY OF OXFORD (United Kingdom)

e WAYNE STATE UNIVERSITY (United States)

Author keywords

Ab initio geometry optimizations; Backbone and side chain conformations; Intramolecular charge transfer; Intramolecular hydrogen bonding; N acetyl L cysteine N methylamide; Side chain stabilization exerted to the backbone

Indexed keywords

ACETYLCYSTEINE DERIVATIVE; AMIDE; METHYL GROUP;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CONFORMATION; ENERGY TRANSFER; GEOMETRY; HYDROGEN BOND;

EID: 0035805428 PISSN: 01661280 EISSN: None Source Type: Journal
DOI: 10.1016/S0166-1280(01)00350-5 Document Type: Article

Times cited : (31)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.