Enantiospecific Formal Total Syntheses of (−)-Salicylihalamides A and B from d-Glucose and l-Rhamnose

Two formal chiral pool syntheses of the (−)-salicylihalamides A and B were achieved from commercially available 1,2,5,6-diacetone-d-glucose and l-rhamnose.

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Bibliographic Details
Published inOrganic letters Vol. 5; no. 21; pp. 4007 - 4009
Main Authors Yang, KyoungLang, Haack, Torsten, Blackman, Burchelle, Diederich, Wibke E, Roy, Subho, Pusuluri, Srinivas, Georg, Gunda I
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 16.10.2003
Amer Chemical Soc
Subjects
Bridged Bicyclo Compounds, Heterocyclic - chemical synthesis
Chemistry
Chemistry, Organic
Glucose - analogs & derivatives
Glucose - chemistry
Molecular Structure
Physical Sciences
Rhamnose - chemistry
Science & Technology
Stereoisomerism
CORE
CYTOTOXIC MACROLIDES
SALICYLIHALAMIDE-A
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Summary:Two formal chiral pool syntheses of the (−)-salicylihalamides A and B were achieved from commercially available 1,2,5,6-diacetone-d-glucose and l-rhamnose.
Bibliography:Medline
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1523-7060
1523-7052
DOI:10.1021/ol035630v