Theoretical Analysis of Optical Rotatory Power of Methylcyclohexanone with Treatment of Conformational Equilibria
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/49/12/49_12_3461/_pdf
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3. Conformational Analysis. XI. The Conformers of 2-Chlorocyclohexanone1,3
4. Contribution of side chain chromophores to the optical activity of proteins. Model compound studies. II. p-Hydroxyphenylglycine and p-hydroxyphenylglycinamide
5. Method of analysis of the rotational strength in terms of the contributions from molecular fragments in the CNDO [complete neglect of differential overlap]/2 approximation
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3. Polarizability tensor theory by Green’s function matrix: Circular dichroism and ultraviolet absorption band shape calculations of cyclo(Gly-Pro-Gly-D-Ala-Pro) having β- and γ-turns;The Journal of Chemical Physics;1998-01
4. Vibrational Raman optical activity in (R)-(+)-3-methylcyclohexanone: experimental and ab initio theoretical studies and the origins of the unusual couplets;Journal of the American Chemical Society;1993-08
5. Chromium, molybdenum, and tungsten;Journal of Organometallic Chemistry;1981-12
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