SCOPUS 정보 검색 플랫폼

Volumn , Issue 1, 2000, Pages 22-26

Template directed cyclo-glycosylation: A convenient approach to unsymmetrical isophthalic disaccharide esters. Influence of the spacer in the stereochemistry of the glycosylation

(4) Valverde, Serafín a García, Mercedes a Gómez, Ana M a López, J Cristóbal a

a INSTITUTO DE QUÍMICA ORGÁNICA GENERAL (Spain)

Author keywords

Dialkylstannyl acetals; Disaccharides; Esterification; Intramolecular glycosylations; Thiol esters

Indexed keywords

2 MERCAPTOBENZOTHIAZOLE; ACETAL DERIVATIVE; BENZYL CHLORIDE; CARBOHYDRATE DERIVATIVE; DISACCHARIDE; ESTER DERIVATIVE; ISOPHTHALIC ACID; PHTHALIC ACID DERIVATIVE; THIOESTER; TIN DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONTROLLED STUDY; ESTERIFICATION; GLYCOSYLATION; MOLECULAR INTERACTION; STEREOCHEMISTRY; SYNTHESIS;

EID: 0033983289 PISSN: 09365214 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (23)

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- 13C NMR).

63
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- The phthaloyl esters reported in this paper were prepared in a regioselective manner from the corresponding monosaccharides by means of dibutylstannylidene acetal chemistry under microwave irradiation and details of these transformations will be reported elsewhere.

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