A synthetic pathway to diquinane and angular triquinane systems via an iron carbonyl promoted tandem [6+2] ene type reaction-Reference-Cited by-同舟云学术

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A synthetic pathway to diquinane and angular triquinane systems via an iron carbonyl promoted tandem [6+2] ene type reaction

Published:2010-07 Issue:27-28 Volume:66 Page:4943-4946
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Pearson Anthony J.,Kim Eun Hoo,Sun Huikai

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Murthy, Y.V.S.; Pillai N., 1992, 48, 5331.

2. The development of polyquinane chemistry

3. Synthesis of Polyquinane Natural Products: An Update

4. Studies on the biosynthesis of pentalenolactone. III. Isolation of a biosynthetic intermediate hydrocarbon, pentalenene.

5. Pentalenene biosynthesis and the enzymatic cyclization of farnesyl pyrophosphate: Proof that the cyclization is catalyzed by a single enzyme

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1. Transformations of Peroxide Products of Alkene Ozonolysis;Russian Journal of Organic Chemistry;2019-01

2. Synthesis of C2-Symmetric gem-Difluoromethylenated Angular Triquinanes;The Journal of Organic Chemistry;2017-12-21

3. Recent Progress in the Synthetic Assembly of 2-Cyclopentenones;Synthesis;2013-11-21

4. An asymmetric total synthesis of (+)-pentalenene;Tetrahedron;2013-09

5. The Chemistry of Diene-Iron and Dienyl-Iron Complexes;PATAI'S Chemistry of Functional Groups;2013-03-18

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