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Volumn 50, Issue 37, 2009, Pages 5285-5287

A new, enantioselective synthesis of (+)-isolaurepan

Author keywords

26 syn Disubstituted tetrahydropyrans; Claisen rearrangement; Enantioselective synthesis; Marine toxins

Indexed keywords

ALLYL ALCOHOL; DIAZOMETHANE; ISOLAUREPAN; OXEPANE DERIVATIVE; TETRAHYDROPYRAN DERIVATIVE; TRI O ACETYL DEXTRO GLUCAL; TRIMETHYLSILYLDIAZOMETHANE; UNCLASSIFIED DRUG;

EID: 67650912592     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.07.041     Document Type: Article
Times cited : (22)

References (49)
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    • The use of 3,3-sigmatropic rearrangements of glycals is common strategy employed to have a stereoselective access to C-glycosides and indeed, to 2,6-disubstituted tetrahydropyrans:
    • The use of 3,3-sigmatropic rearrangements of glycals is common strategy employed to have a stereoselective access to C-glycosides and indeed, to 2,6-disubstituted tetrahydropyrans:. Tulshian D.B., and Fraser-Reid B. J. Org. Chem. 49 (1984) 518
    • (1984) J. Org. Chem. , vol.49 , pp. 518
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    • note
    • Although d-glucal is commercially available, tri-O-acetyl-d-glucal is much cheaper and should be used for large-scale synthesis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.