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Volumn 53, Issue 39, 2014, Pages 10381-10385

Furanosyl oxocarbenium ion stability and stereoselectivity

Author keywords

carbohydrates; conformation analysis; density functional calculations; Lewis acids; reaction mechanisms

Indexed keywords

ADDITION REACTIONS; CARBOHYDRATES; DENSITY FUNCTIONAL THEORY; FREE ENERGY; POTENTIAL ENERGY; QUANTUM CHEMISTRY; STEREOSELECTIVITY; SUBSTITUTION REACTIONS;

EID: 84953331590     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201405477     Document Type: Article
Times cited : (64)

References (30)
  • 28
    • 66249145069 scopus 로고    scopus 로고
    • N1 reactions on glycosyl oxocarbenium ions are notoriously difficult because these require the use of counterions, both on the side of the electrophile and the nucleophile, to prevent the barrierless formation of noncharged species. See for example, Ref. [8a]
    • N1 reactions on glycosyl oxocarbenium ions are notoriously difficult because these require the use of counterions, both on the side of the electrophile and the nucleophile, to prevent the barrierless formation of noncharged species. See for example, Ref. [8a];, D. M. Whitfield, Adv. Carbohydr. Chem. Biochem. 2009, 62, 83-159.
    • (2009) Adv. Carbohydr. Chem. Biochem. , vol.62 , pp. 83-159
    • Whitfield, D.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.