Please use this identifier to cite or link to this item:
192.168.6.56/handle/123456789/74415
Title: | Organic Chemistry from Retrosynthesis to Asymmetric Synthesis |
Authors: | Šunjić, Vitomir Peroković, Vesna Petrović |
Keywords: | Chemistry |
Issue Date: | 2016 |
Publisher: | Springer International Publishing Switzerland |
Description: | There is a substantial didactic difference between retrosynthetic analysis and asymmetric synthesis. This difference refers to the chiral target molecules. They are regarded as racemic in “two-dimensional” retrosynthesis, but one enantiomer is the target in asymmetric synthesis. Retrosynthesis without considering the absolute configuration anticipates the synthesis of racemic target molecules, while asymmetric synthesis leads to the preferred enantiomers. Concerning the conceptual and practical difference between retrosynthesis without consideration of the stereochemistry and asymmetric synthesis of optically pure target molecules, we underline considering asymmetric synthesis as a “departure to the third dimension.” |
URI: | http://10.6.20.12:80/handle/123456789/74415 |
ISBN: | 978-3-319-29926-6 |
Appears in Collections: | Chemistry |
Files in This Item:
File | Description | Size | Format | |
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2016_Book_OrganicChemistryFromRetrosynth.pdf | 18.75 MB | Adobe PDF | View/Open |
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