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Thionation of Optically Pure N‑C Axially Chiral Quinazolin-4-one Derivatives with Lawesson’s Reagent
The reaction of various optically pure N–C axially chiral quinazolin-4-one derivatives with Lawesson’s reagent proceeded without a marked decrease in optical purity to give optically active quinazoline-4-thione derivatives (93–99% ee) possessing a high rotational barrier in good yields.
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Published in: | Journal of organic chemistry 2021-01, Vol.86 (1), p.709-715 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The reaction of various optically pure N–C axially chiral quinazolin-4-one derivatives with Lawesson’s reagent proceeded without a marked decrease in optical purity to give optically active quinazoline-4-thione derivatives (93–99% ee) possessing a high rotational barrier in good yields. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/acs.joc.0c02319 |