Two step synthesis of 3,7,7-trimethyl-1,3,5-cycloheptatriene from Delta(3)-carene
3,7,7-trimethyl-1,3,5-cycloheptatriene was obtained in 74% overall yield when adducts from ene reaction between Delta(3)-carene and N-sulphinyl arenesulphonamides are reacted with hexamethyl disilazane at 80 degrees C.
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Published in | Phosphorus and sulfur and the related elements Vol. 101; no. 1-4; pp. 287 - 289 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
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Taylor & Francis
01.04.1995
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Subjects | |
Online Access | Get more information |
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Summary: | 3,7,7-trimethyl-1,3,5-cycloheptatriene was obtained in 74% overall yield when adducts from ene reaction between Delta(3)-carene and N-sulphinyl arenesulphonamides are reacted with hexamethyl disilazane at 80 degrees C. |
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ISSN: | 0308-664X |
DOI: | 10.1080/10426509508042529 |