Conformational interactions between a phenyl ring and a side-chain halide substituent: A 1H NMR and molecular mechanics study of some 2-aryl-1-halopropanes-Reference-Cited by-同舟云学术

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Conformational interactions between a phenyl ring and a side-chain halide substituent: A 1H NMR and molecular mechanics study of some 2-aryl-1-halopropanes

Published:1990-01 Issue:6 Volume:46 Page:957-965
ISSN:0584-8539
Container-title:Spectrochimica Acta Part A: Molecular Spectroscopy
language:en
Short-container-title:Spectrochimica Acta Part A: Molecular Spectroscopy

Author:

Cook Michael J.,Howe Trevor J.

Publisher

Elsevier BV

Subject

General Engineering

Reference17 articles.

1. Rotational equilibria in 2-aryl--propanols, 2-aryl--propyl methyl ethers and 2-aryl--propyl acetates. Trends consistent with a CH---O hydrogen bond

2. The effect of -substituents on the comformational behaviour of aromatic sidechains

3. The contrasting comformational behaviour of 5-aryl-5-methyl-1,3-dioxanes and 1-aryl-1-methylcyclohexahes

4. Reduction of Carbonyl Compounds by Sodium Borohydride Adsorbed on Alumina

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. Determination of rotamer populations and related parameters from NMR coupling constants: a critical review;Analytical and Bioanalytical Chemistry;2004-03-01

2. Long-range substituent effects on conformational equilibria;Journal of Molecular Structure;1990-11

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