Halogen catalyzed acetylenic oxy-cope rearrangement in N-methyl-2-pyrrolidone solvent a new industrial process for pseudoionone and its analogues-Reference-Cited by-同舟云学术

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Halogen catalyzed acetylenic oxy-cope rearrangement in N-methyl-2-pyrrolidone solvent a new industrial process for pseudoionone and its analogues

Published:1980-01 Issue:14 Volume:21 Page:1347-1350
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fujita Yoshiji,Onishi Takashi,Hino Kenichi,Nishida Takashi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. T. Onishi, Y. Fujita, T. Nishida, Synthesis, will be published.

2. Ring expansion by siloxy-Cope rearrangement

3. [3,3]Sigmatropic rearrangements of 1,5-diene alkoxides. Powerful accelerating effects of the alkoxide substituent

4. A NOVEL ETHYNYLATION OF α-SUBSTITUTED MESITYL OXIDES

5. Solvent Assisted Oxy-Cope Rearrangement of Diastereomeric 1,5-Hexaden-3-ols. A New Industrial Process for Polyprenyl Ketones

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1. Epoxides from Myrcene: New Versatile Tools for the Synthesis of Functionalized Acyclic Terpenoids;Synthetic Communications;1999-11

2. One or More CH, CC, and/or CC Bonds Formed by Rearrangement;Comprehensive Organic Functional Group Transformations;1995

3. References to Volume 3;Comprehensive Organic Functional Group Transformations;1995

4. Ketones: α,β-Unsaturated Ketones;Comprehensive Organic Functional Group Transformations;1995

5. References to Volume 1;Comprehensive Organic Functional Group Transformations;1995

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