SCOPUS 정보 검색 플랫폼

Volumn , Issue 8, 2001, Pages 1263-1267

A novel approach to both the enantiomers of potent glycosidase inhibitor isofagomine via PET-promoted cyclization of 1-[benzyl(trimethylsilylmethyl)amino]-1,4,5-trideoxy-2,3-O-(1- methylethylidene)-threo-pent-4-ynitol

(2) Pandey, G a Kapur, M a

a NATIONAL CHEMICAL LABORATORY (India)

Author keywords

1 N iminosugars; Glycosidase inhibitors; Isofagomine; Photoinduced electron transfer (PET); trimethylsilylmethylamine radical cation

Indexed keywords

ACETYLENE; POSITIVE IONS;

ENANTIOMERS; GLYCOSIDASE;

SYNTHESIS (CHEMICAL);

1 [BENZYL (TRIMETHYLSILYLMETHYL)AMINO] 1,4,5 TRIDEOXY 2,3 O (1 METHYLETHYLIDENE) THREO PENT 4 YNITOL; CARBOHYDRATE DERIVATIVE; CATION; GLYCOSIDASE INHIBITOR; IMINE; ISOFAGOMINE; RADICAL; TRIMETHYLSILYL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; DRUG STRUCTURE; ELECTRON TRANSPORT; ENANTIOMER; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

EID: 0034957223 PISSN: 00397881 EISSN: None Source Type: Journal
DOI: 10.1055/s-2001-15063 Document Type: Article

Times cited : (38)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.