Hyperconjugation Involving Strained Carbon–Carbon Bonds. Structural Analysis of Ester and Ether Derivatives and One-Bond 13C–13C Coupling Constants of α- and β-Nopinol-Reference-Cited by-同舟云学术

Hyperconjugation Involving Strained Carbon–Carbon Bonds. Structural Analysis of Ester and Ether Derivatives and One-Bond 13C–13C Coupling Constants of α- and β-Nopinol

Published:2012-12-20 Issue:2 Volume:78 Page:311-319
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yeoh Shinn Dee¹,Skene Colin E.¹,White Jonathan M.¹

Affiliation:

1. School of Chemistry and Bio-21 Institute, University of Melbourne, Parkville, Victoria 3010, Australia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo3020243

Reference48 articles.

1. A Silyl Substituent Can Dictate a Concerted Electrocyclic Pathway: Inward Torquoselectivity in the Ring Opening of 3-Silyl-1-cyclobutene

2. Stereoelectronic effects in the formation of 5- and 6-membered rings: the role of Baldwin's rules

3. The Anomeric Effect and Related Stereoelectronic Effects at Oxygen

4. Stereoelectronic Substituent Effects

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