Synthesis of Z-alkenes from alkenylcatecholboranes through reaction with RMgX and I < inf > 2 < /inf > induced rearrangement

dc.contributor.author Periasamy, Mariappan
dc.contributor.author Bhanu Prasad, A. S.
dc.contributor.author Suseela, Yantrapragada
dc.date.accessioned 2022-03-27T09:11:32Z
dc.date.available 2022-03-27T09:11:32Z
dc.date.issued 1995-02-27
dc.description.abstract Addition of RMgX and BrMg (CH2) nMgBr reagents to alkenylcatecholborane followed by iodine induced rearrangement and oxidation provided Z-olefins and Z-olefinic alcohols in moderate to good yields. This procedure is advantageous over the previous methods of synthesis of Z-olefins from alkenylboranes since the alkyl groups which are not available through hydroborations can be also utilized. © 1995.
dc.identifier.citation Tetrahedron. v.51(9)
dc.identifier.issn 00404020
dc.identifier.uri 10.1016/0040-4020(95)00023-2
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/0040402095000232
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12561
dc.title Synthesis of Z-alkenes from alkenylcatecholboranes through reaction with RMgX and I < inf > 2 < /inf > induced rearrangement
dc.type Journal. Article
dspace.entity.type
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