Studies towards the synthesis of bielschowskysin. Construction of the highly functionalized bicyclo[3.2.0]heptane segment
Author:
Affiliation:
1. Department of Organic Chemistry
2. Indian Association for the Cultivation of Science
3. Jadavpur
4. India
Abstract
A stereocontrolled approach for the construction of a highly functionalized bicyclo[3.2.0]heptane derivative embodying the bridged lactone present in the diterpene bielschowskysin is reported.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2015/OB/C4OB02182G
Reference34 articles.
1. Bielschowskysin, a Gorgonian-Derived Biologically Active Diterpene with an Unprecedented Carbon Skeleton
2. Progress toward the Total Synthesis of Bielschowskysin: A Stereoselective [2 + 2] Photocycloaddition
3. Stereocontrolled entry to the tricyclo[3.3.0]oxoheptane core of bielschowskysin by a [2+2] cycloaddition of an allene-butenolide
4. An Expedient Synthesis of a Functionalized Core Structure of Bielschowskysin
5. A Non-Photochemical Approach to the Bicyclo[3.2.0]heptane Core of Bielschowskysin
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