Acyclic stereoselection for 1,2-diol systems via vinyl acetal rearrangement: control of relative stereochemistry in the rearrangement of 2,2,4-trimethyl-1,3-dioxolan-4-yl prop-1-enyl ethers to 2,3-dimethyl-3,4-(isopropylidenedioxy)butanals-Reference-Cited by-同舟云学术

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Acyclic stereoselection for 1,2-diol systems via vinyl acetal rearrangement: control of relative stereochemistry in the rearrangement of 2,2,4-trimethyl-1,3-dioxolan-4-yl prop-1-enyl ethers to 2,3-dimethyl-3,4-(isopropylidenedioxy)butanals

Published:1988-04 Issue:9 Volume:53 Page:1860-1862
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Frauenrath Herbert,Runsink Jan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00244a004

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis of New Polyfunctional Cyclic Ketals Based on Substituted 4-Methylene-1,3-dioxolanes;Doklady Chemistry;2024-01-31

2. Addition of Alcohols to 4-Methylene-1,3-dioxolanes;Russian Journal of General Chemistry;2023-10

3. Isomerization of Alkenes;Comprehensive Organic Transformations;2018-02-28

4. Formation of Aldehydes and Ketones by Rearrangements;Comprehensive Organic Transformations;2018-02-28

5. Acid catalyzed rearrangement of vinyl and ketene acetals;Tetrahedron;2014-02

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