Ring Opening of Bicyclo[n.1.0]alkanones to 2-Cycloalkanone-1,3-diyls. Why Does Oxyallyl Diradical Formation Require Less Energy from Bicyclo[3.1.0]hexan-6-ones than from Bicyclo[1.1.0]butan-2-ones?-Reference-Cited by-同舟云学术

Ring Opening of Bicyclo[n.1.0]alkanones to 2-Cycloalkanone-1,3-diyls. Why Does Oxyallyl Diradical Formation Require Less Energy from Bicyclo[3.1.0]hexan-6-ones than from Bicyclo[1.1.0]butan-2-ones?

Published:1996-01-01 Issue:17 Volume:118 Page:4159-4166
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Hrovat David A.¹,Rauk Arvi¹,Sorensen T. S.¹,Powell Helen K.¹,Borden Weston Thatcher¹

Affiliation:

1. Contribution from the Departments of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195-1700, and University of Calgary, Calgary, Alberta T2N 1N4, Canada

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja954296y

Reference26 articles.

1. A new synthesis of in situ cyclopropanones and the observation of a thermal cyclopropanone–dienol rearrangement

2. Preparation and Structure Investigations of Simple Bicyclo[1.1.0]butanones

3. Attempted Generation of an Observable Ethano-Bridged (Cyclopentyl) Oxyallyl. The Pericyclic Nature of an Oxyallyl-Oxyallyl Dimerization Reaction

4. Ab initio computational study of methano- and ethano-bridged derivatives of oxyallyl

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