Allylchlorotins of the type R3-nAllSnCln (R alkyl or All; All CH2CHCH2 or cis/trans-CH3CHCHCH2, n 1-3) undergo uncatalyzed coupling with acyl chlorides under mild conditions. This reaction as well as the corresponding addition reaction to ketones are much faster when Cl is replaced by NCS group in the organotin derivative.

Allylchlorotins as allylating agents of acyl chlorides

GAMBARO, ALESSANDRO;PERUZZO, VALERIO;MARTON, DANIELE
1983

Abstract

Allylchlorotins of the type R3-nAllSnCln (R alkyl or All; All CH2CHCH2 or cis/trans-CH3CHCHCH2, n 1-3) undergo uncatalyzed coupling with acyl chlorides under mild conditions. This reaction as well as the corresponding addition reaction to ketones are much faster when Cl is replaced by NCS group in the organotin derivative.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2489773
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