Configurational and Conformational Analysis of Chiral Molecules Using IR and VCD Spectroscopies: Spiropentylcarboxylic Acid Methyl Ester and Spiropentyl Acetate-Reference-Cited by-同舟云学术

Configurational and Conformational Analysis of Chiral Molecules Using IR and VCD Spectroscopies: Spiropentylcarboxylic Acid Methyl Ester and Spiropentyl Acetate

Published:2002-10-23 Issue:23 Volume:67 Page:8090-8096
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Devlin F. J.¹,Stephens P. J.¹,Österle C.¹,Wiberg K. B.¹,Cheeseman J. R.¹,Frisch M. J.¹

Affiliation:

1. Department of Chemistry, University of Southern California, Los Angeles, California 90089-0482, Department of Chemistry, Yale University, New Haven, Connecticut 06511, and Gaussian Inc., 140 Washington Avenue, North Haven, Connecticut 06473

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo020225n

Reference22 articles.

1. Stereochemistry of the Deamination of Spiropentylamine

2. Determination of the structure of chiral molecules using ab initio vibrational circular dichroism spectroscopy

3. (b) Stephens, P. J.; Devlin, F. J.; Aamouche, A. InChirality: Physical Chemistry; Hicks, J. M., Ed.; ACS Symposium Series 810; American Chemical Society: Washington, DC, 2002; pp 18−33.

4. Determination of Absolute Configuration Using Vibrational Circular Dichroism Spectroscopy: The Chiral Sulfoxide 1-(2-methylnaphthyl) Methyl Sulfoxide

5. Determination of absolute configuration using vibrational circular dichroism spectroscopy: the chiral sulfoxide 1-thiochroman S-oxide

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