Complication of Graphic Representation of Three-Dimentional Structure
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- Kirihara Masayuki
- Shizuoka Institute of Science & Technology
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- Mochizuki Tomohiro
- Shizuoka Institute of Science & Technology
Bibliographic Information
- Other Title
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- 立体表記法の混乱
Abstract
Structural diagrams which depict stereochemistry have been used in the structural drawings for organic chemistry. In general, plain lines depict bonds approximately in the plane of the drawing; bonds to atoms above the plane are shown with a bold wedge (starting from an atom in the plane of the drawing at the narrow end of the wedge); and bonds to atoms below the plane are shown by broken lines. In the cases of the broken lines, they are typically used in three different ways. 1. Narrow end as being in the plane of the drawing (Method A). 2. Short parallel lines (Method B). 3. Narrow end as furthest from the viewer (Method C). We investigated which method has been mainly used. Although IUPAC recommends Method B, most chemists have recently used Method A in the chemical journals.
Journal
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- Proceedings of the Symposium on Progress in Organic Reactions and Syntheses
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Proceedings of the Symposium on Progress in Organic Reactions and Syntheses 34 (0), 76-76, 2008
Division of Organic Chemistry, The Pharmaceutical Society of Japan
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Details 詳細情報について
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- CRID
- 1390001205636147712
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- NII Article ID
- 130006998808
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- Text Lang
- ja
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed