Expedient asymmetric synthesis of a functionalized 5-7-6 fused tricyclic skeleton present in caribenol A through ring opening-ring closing metathesis of a norbornene derivative-Reference-Cited by-同舟云学术

Expedient asymmetric synthesis of a functionalized 5-7-6 fused tricyclic skeleton present in caribenol A through ring opening-ring closing metathesis of a norbornene derivative

Published:2009-09 Issue:37 Volume:50 Page:5277-5279
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Mondal Sujit,Yadav Ram N.,Ghosh Subrata

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Caribenols A and B, Sea Whip Derived Norditerpenes with Novel Tricarbocyclic Skeletons

2. Tuberculosis: Commentary on a Reemergent Killer

3. Sequential Metathesis in Oxa‐ and Azanorbornene Derivatives

4. Ring-Rearrangement Metathesis

5. Rearrangement of bicyclo[2.2.1]heptane ring systems by titanocene alkylidene complexes to bicyclo[3.2.0]heptane enol ethers. Total synthesis of (.+-.)-.DELTA.9(12)-capnellene

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4. Recent applications of ring-rearrangement metathesis in organic synthesis;Beilstein Journal of Organic Chemistry;2015-10-07

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