A facile functionalization of the isopropylidene terminus of isoprenoids. Application to the synthesis of terminal trans allylic alcohols-Reference-Cited by-同舟云学术

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A facile functionalization of the isopropylidene terminus of isoprenoids. Application to the synthesis of terminal trans allylic alcohols

Published:1978-01 Issue:46 Volume:19 Page:4539-4542
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Masaki Yukio,Hashimoto Kinji,Kaji Kenji

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Stereoselective Synthesis of Trisubstituted Olefins

2. New approach for the stereocontrolled synthesis of acyclic terpenes

3. STEREOSELECTIVE SYNTHESIS OF TRISUBSTITUTED OLEFINS VIA π-ALLYLIC NICKEL BROMIDE COMPLEXES WITH FUNCTIONAL GROUP

4. A New, Highly Stereoselective Synthesis of alltrans-Geranylgeraniol

5. Stereoselective Trans-trisubstituted olefin synthesis via rearrangement of allylic sulfonium ylides

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1. Molecular Rearrangements of Highly Functionalized Terpenes. An Unique Reactivity of Bicyclic Framework and Polienic Chain Inhibition under Superacidic Treatment;Chemistry Journal of Moldova;2013-12

2. Benzenesulfenyl Chloride;Encyclopedia of Reagents for Organic Synthesis;2013-04-22

3. Benzenesulfenyl Chloride;Fieser and Fieser's Reagents for Organic Synthesis;2011-08-15

4. Benzenesulfenyl Chloride;Fieser and Fieser's Reagents for Organic Synthesis;2009-12-15

5. Benzenesulfenyl Chloride;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15

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