Stereoselective synthesis of tetrasubstituted alkenes via a sequential carbocupration and a new sulfur–lithium exchange
2012 ◽
Vol 8
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pp. 2202-2206
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Keyword(s):
We have designed a new sequential carbocupration and sulfur–lithium exchange that leads stereo- and regioselectively to trisubstituted alkenyllithiums. Subsequent trapping with various electrophiles yields tetrasubstituted olefins with good control of the double-bond geometry (E/Z ratio up to 99:1). The novel sulfur–lithium exchange could be extended to the stereoselective preparation of Z-styryl lithium derivatives with almost complete retention of the double-bond geometry.
Keyword(s):
2009 ◽
Vol 49
(3)
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pp. 377-384
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Keyword(s):
2012 ◽
Vol 51
(15)
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pp. 3699-3702
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