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Stille Cross-Couplings of Unactivated Secondary Alkyl Halides Using Monoorganotin Reagents

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NIAID Data Ecosystem2026-03-06 收录
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https://figshare.com/articles/dataset/Stille_Cross_Couplings_of_Unactivated_Secondary_Alkyl_Halides_Using_Monoorganotin_Reagents/3304210
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The first catalyst that achieves Stille cross-couplings of secondary (as well as primary) alkyl halides has been developed. The method employs easily handled and inexpensive catalyst components (NiCl2 and 2,2‘-bipyridine) and, through the use of monoorganotin reagents, avoids the formation of toxic and difficult-to-remove triorganotin side products.
创建时间:
2016-05-06
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