ChemInform Abstract: Stereoselective Total Synthesis of 4-((3S,5R)-3,5-Dihydroxynonadecyl)phenol

The stereoselective total synthesis of (I) is achieved via two alternative strategies involving either a Prins cyclization as the key step (28% overall yield) or a 1,3‐syn reduction of a β‐hydroxy ketone (30% overall yield).

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Bibliographic Details
Published inChemInform Vol. 45; no. 30; p. no
Main Authors Yadav, J. S., Reddy, P. Adi Narayana, Kumar, A. Suman, Prasad, A. R., Reddy, B. V. Subba, Al Ghamdi, Ahmad Alkhazim
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 29.07.2014
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
Subjects
Beta
other natural products
structure (organic substances)
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Summary:The stereoselective total synthesis of (I) is achieved via two alternative strategies involving either a Prins cyclization as the key step (28% overall yield) or a 1,3‐syn reduction of a β‐hydroxy ketone (30% overall yield).
Bibliography:istex:F6051B4517DA17F7389779D96C9159FD52CF1207
ArticleID:CHIN201430214
ark:/67375/WNG-5L7R8NWX-1
ISSN:0931-7597
1522-2667
DOI:10.1002/chin.201430214