Co-crystallization of pentacyclododecane acetate rotamers of opposite chirality: effects of steric interactions and negative hyperconjugation on molecular structure-Reference-Cited by-同舟云学术

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Co-crystallization of pentacyclododecane acetate rotamers of opposite chirality: effects of steric interactions and negative hyperconjugation on molecular structure

Published:2003-06 Issue:1-3 Volume:654 Page:139-143
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Seidl P.R,Sabino J.R,Castellano E.E,Mascarenhas Y.P,Costa V.E.U,Alifantes J,de Paula e Silva C.H.T,Dias J.F

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference20 articles.

1. Skeletal Rearrangements in Reactions of Isodrin and Endrin

2. Evaluation of lipase from Candida rugosa in the resolution of endo-(±)-1,8,9,10,11,11-hexachloropentacyclo[6.2.1.13,6.02,7.05,9]dodecan-4-alcohol

3. Conformational effects on properties of half-cage compounds

4. Ultrashort nonbonded hydrogen...hydrogen distance in a half-cage pentacyclododecane

Cited by 2 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. Congested molecules. Where is the steric repulsion? An analysis of the electron density by the method of interacting quantum atoms;International Journal of Quantum Chemistry;2013-05-22

2. 17O NMR investigation of rigid polycyclic systems: experimental and calculated chemical shifts;Journal of Molecular Structure;2004-09

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