Synthesis of allylic sulfonic acids via regioselective Pd-catalyzed allylic substitutions of Na 2 SO 3
摘要:
Palladium-catalyzed allylic sulfonations of the linear allylic carbonates with sodium sulfite (Na2SO3) were accomplished under mild conditions. This method gave allylic sulfonic acids in good to excellent yields with high level of regioselectivities. (C) 2015 Elsevier Ltd. All rights reserved.
A highly regioselective palladium-catalyzedallylic alkylation of fluorobis(phenylsulfonyl)methane has been studied. Using different allylic carbonates, a variety of terminal mono-fluoromethylated compounds were achieved in 85–99% yields with high regioselectivities.
A One-Pot Palladium-Catalyzed Allylic Alkylation and Wittig Reaction of Phosphorus Ylides
作者:Wen-Bo Liu、Hu He、Li-Xin Dai、Shu-Li You
DOI:10.1002/chem.201000316
日期:2010.7.5
Put a(n) (y)lid(e) on it! The one‐pot palladium‐catalyzed allylic alkylation and Wittigreaction of phosphorus ylides with various aldehydes and ketenes has been realized, which produce skipped dienes, including trisubstituted alkenes and tetrasubstituted allenes, respectively (see scheme), in moderate to good overall yields.
of readily available aminoacids, which is not only an oxygen nucleophile but also a nitrogen nucleophile, in palladium-catalyzed allylic substitution is realized under mild conditions. The chemoselectivity and multiple allylation are controlled by adjusting the reaction conditions. This represents the first example of this convenient access to valuable N,O-diallylated aminoacids. Under the title conditions