Threshold Rotational Mechanisms and Enantiomerization Barriers of Polyarylvinyl Propellers

Author:

Rappoport Zvi1,Biali Silvio E.1

Affiliation:

1. Department of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel

Publisher

American Chemical Society (ACS)

Subject

General Medicine,General Chemistry

Reference48 articles.

1. Reviews:  Mislow, K.; Gust, D.; Finocchiaro, P.; Boettcher, R. J.Fortschr. Chem. Forschr.1974, 47, 1. Mislow, K.Acc. Chem. Res.1976,9, 26. Meurer, K. P.; Vögtle, F.Top. Curr. Chem.1985,127, 1. Willem. R.; Gielen, M.; Hoogzand, C.; Pepermans, H.Advances Dyn. Stereochemistry; Gielen, M., Ed.; Academic Press:  New York, 1985; Vol. 1, p 207.

2. Syntheses of Azulene Analogues of Triphenylmethyl Cation: Extremely Stable Hydrocarbon Carbocations and the First Example of a One-Ring Flip as the Threshold Rotation Mechanism for Molecular Propellers

3. Analysis of isomerization in compounds displaying restricted rotation of aryl groups

4. Chromatographic resolution of perchlorotriphenylamine on (+)-poly(triphenylmethyl methacrylate)

5. Mislow, K.Chemtracts:  Org. Chem.1989,2, 151.

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