Origin of Stereoselectivity in the (4 + 3) Cycloadditions of Chiral Alkoxy Siloxyallyl Cations with Furan-Reference-Cited by-同舟云学术

Origin of Stereoselectivity in the (4 + 3) Cycloadditions of Chiral Alkoxy Siloxyallyl Cations with Furan

Published:2010-01-11 Issue:3 Volume:12 Page:444-447
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Krenske Elizabeth H.¹,Houk K. N.¹,Harmata Michael¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, and Department of Chemistry, University of Missouri—Columbia, Columbia, Missouri 65211

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol902591k

Reference18 articles.

1. The Cycloaddition of Allyl Cations to 1,3-Dienes: General Method for the Synthesis of Seven-Membered Carbocycles. New Synthetic Methods(40)

2. Cycloaddition reactions of vinyl oxocarbenium ions

3. Ambiphilic reactivity of 1,1-dimethoxyacetone

4. Chiral Allyl Cations in Cycloadditions to Furan: Synthesis of 2-(1′-Phenylethoxy)-8-oxabicyclo[3.2.1]oct-6-en-3-one in High Enantiomeric Purity

5. Chiral Allyl Cations Are Captured by Furan with 100 % Stereoselectivity: Synthesis of Enantiopure 2-Alkoxy-8-oxabicyclo[3.2.1]oct-6-en-3-ones by Low-Temperature [4+3] Cycloaddition

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