Novel autoxidation and Michael addition of a butenolide-containing sugar leading to a C-branched-chain glucopyranosidulose, and X-ray structure of intermediates

Carbohydrate Research

Volumn 338, Issue 17, 2003, Pages 1737-1743

  Liu, Hong Min ^a   Zhang, Fuyi ^a   Zhang, Jianye ^a   Li, Shi ^a  

^a ZHENGZHOU UNIVERSITY   (China)

Author keywords

2 Oxoglucopyranoside; Autoxidation; Butenolide containing sugar

Indexed keywords

ADDITION REACTIONS; IONS; OXIDATION;

AUTOXIDATION;

SUGARS;

ACID; BASE; BUTENOLIDE; CARBOHYDRATE DERIVATIVE; GAMMA LACTONE DERIVATIVE; GLUCOPYRANOSIDE; HYDROXIDE; ION; MALONIC ACID DERIVATIVE; METHYL 4,4A,6,8,9A,9B HEXAHYDRO 6 METHOXY 8 OXO 2 PHENYLFURO[2',3':4,5]PYRANO[3,2 D] 1,3 DIOXIN 7 CARBOXYLATE; METHYL 4,4A,6,8,9A,9B HEXAHYDRO 9A HYDROXY 6 METHOXY 8 OXO 2 PHENYLFURO[2',3':4,5]PYRANO[3,2 D] 1,3 DIOXIN 7 CARBOXYLATE; METHYL 4,6 O BENZYLIDENE 2 C METHOXYCARBONYLMETHYL ALPHA RIBOHEXOPYRANOSID 3 ULOSE; METHYL 4,6 O BENZYLIDENE ALPHA GLUCOPYRANOSID 2 ULOSE; PYRANOSIDE; SUGAR; UNCLASSIFIED DRUG; WATER;

ALDOL REACTION; ARTICLE; AUTOOXIDATION; CHEMICAL STRUCTURE; CONJUGATE; CULTURE MEDIUM; MICHAEL ADDITION; PRIORITY JOURNAL; X RAY;

EID: 0042845752     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0008-6215(03)00257-X     Document Type: Article

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