Destannylative Pummerer-type rearrangement of 1-(tributylstannyl)-1-(phenylsulfinyl)- cyclopropane and -ethene.
1-(Tributylstannyl)-1-(phenylsulfinyl)-cyclopropane and -ethene were found to react with acyl chlorides to provide the corresponding 1-acyloxy-1-(phenylthio)-cyclopropanes and -ethenes. The reaction involves the Pummerer-type rearrangement with loss of the tributylstannyl group. © 1993.
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| Main Authors: | , , |
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| Format: | Article |
| Published: |
2018
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| Subjects: | |
| Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/22533 |
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| Institution: | Mahidol University |