d-orbital stereoelectronic control of the stereochemistry of SN2′ displacements by organocuprate reagents
摘要:
The anti stereochemistry observed in organocuprate S N2′ displacements can be rationalized as a stereoelectronic effect arising from "bidentate" binding involving a d orbital of nueleophilic copper and π* and σ* orbitals of the substrate. The extension of this idea to other reactions of organocuprates including additions to acetylenes and enones is discussed.
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DOI:
10.1016/0040-4039(84)80008-8
被引量:
年份:
1984
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来源期刊
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2010
被引量:162
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