Synthesis and Structure of Cyclopropano-Annelated Homosesquinorbornene Derivatives Containing Pyramidalized Double Bonds: Evidence for the Sterical Effect of a Cyclopropyl Group on the Degree of CC Double-Bond Pyramidalization-Reference-Cited by-同舟云学术

Synthesis and Structure of Cyclopropano-Annelated Homosesquinorbornene Derivatives Containing Pyramidalized Double Bonds: Evidence for the Sterical Effect of a Cyclopropyl Group on the Degree of CC Double-Bond Pyramidalization

Published:2005-06-16 Issue:14 Volume:70 Page:5403-5408
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Saracoglu Nurullah¹,Talaz Oktay¹,Azizoglu Akín¹,Watson William H.¹,Balci Metin¹

Affiliation:

1. Department of Chemistry, Atatürk University, 25240 Erzurum, Turkey, Department of Chemistry, Balikesir University, 10100 Balikesir-Turkey, Department of Chemistry, Texas Christian University, Fort Worth, Texas 76129, and Department of Chemistry, Middle East Technical University, 06531 Ankara, Turkey

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo050327o

Reference49 articles.

1. Pyramidalized alkenes

2. Nonplanar alkenes and carbonyls: a molecular distortion which parallels addition stereoselectivity

3. Double-Bond Geometry of Norbornene: Neutron Diffraction Measurement of a Derivative at 15 K

4. Double-bond geometry in norbornene, sesquinorbornenes, and related compounds: a high-level quantum chemical investigation

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