キラリティー，RS-ステレオジェニシティ，スクレラリティを考慮した立体異性体の数え上げ

藤田 眞作

doi:10.11545/ciqs.2007.0.J14.0

30th Symposium on Chemical Information and Computer Sciences, Kyoto

DOI https://doi.org/10.11545/ciqs.2007.0.J14.0

Conference information

Host: Division of Chemical Information and Computer Science, The Chemical Society of Japan

Co-host: The Pharmaceutical Society of Japan, Japan Society for Bioscience, Biotechnology, and Agrochemistry, The Japan Society for Analytical Chemistry, Society of Computer Chemistry, Japan, Japanese Society for Information and Systems in Education (Approaval)

Oral Session

Enumeration of Stereoisomers by Considering Chirality, RS-Stereogenicity, and Sclerality

*Fujita Shinsaku

Author information

Keywords: enumeration, stereoisomer, chirality, stereogenicity, promolecule

CONFERENCE PROCEEDINGS FREE ACCESS

Pages J14

Details

Abstract

Promolecules derived from a given skelelton are regarded as RS-stereoisomers and they are categorized into five types (Types I--V) by means of chirality, RS-stereogenicity, and sclerality. They are generally enumerated under the actions of three subgroups (the maximum point subgroup, the maximum RS-permutation group, and the maximum lignd-inversion group). The general method is applied to allene and methane skeletons.

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