SCOPUS 정보 검색 플랫폼

Volumn 65, Issue 18, 2000, Pages 5547-5557

Synthesis of 3,7-anhydro-D-glycero-D-ido-octitol 1,5,6-trisphosphate as an IP3 receptor ligand using a radical cyclization reaction with a vinylsilyl tether as the key step. Conformational restriction strategy using steric repulsion between adjacent bulky protecting groups on a pyranose ring

(4) Shuto, Satoshi a Yahiro, Yumi a Ichikawa, Satoshi a Matsuda, Akira a

a HOKKAIDO UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

3,7 ANHYDRO DEXTRO GLYCERO DEXTRO IDO OCTITOL A,5,6 TRIPHOSPHATE; GLUCOPYRANOSIDE; HYDROXYL GROUP; INOSITOL 1,4,5 TRISPHOSPHATE; PHOSPHATE; PHOSPHORAMIDIC ACID DERIVATIVE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

ARTICLE; BINDING AFFINITY; CHEMICAL STRUCTURE; CONFORMATION; CONFORMATIONAL TRANSITION; CYCLIZATION; OXIDATION; PHOSPHORYLATION; STEREOSPECIFICITY; SYNTHESIS;

EID: 0033828729 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo0002339 Document Type: Article

Times cited : (48)

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- (1995) Mol. Pharmacol. , vol.47 , pp. 1204-1211
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