Premium
Diversity‐Orientated Stereoselective Synthesis through Pd‐Catalyzed Switchable Decarboxylative C−N/C−S Bond Formation in Allylic Surrogates
Author(s) -
Deng Lei,
Kleij Arjan W.,
Yang Weibo
Publication year - 2018
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201805295
Subject(s) - allylic rearrangement , stereoselectivity , nucleophile , chemistry , synthon , catalysis , combinatorial chemistry , surface modification , substrate (aquarium) , tsuji–trost reaction , ligand (biochemistry) , substitution reaction , stereochemistry , organic chemistry , receptor , biology , ecology , biochemistry
Abstract Switchable catalytic transformation of reactants can be a powerful approach towards diversity‐orientated synthesis from easily available molecular synthons. Herein, an endogenous ligand‐controlled, Pd‐catalyzed allylic substitution allowing for either selective C−N or C−S bond formation using vinylethylene carbonates (VECs) and N ‐sulfonylhydrazones as coupling partners has been developed. This versatile methodology provides a facile, divergent route for the highly chemo‐ and stereoselective synthesis of functional allylic sulfones or sulfonohydrazides. The newly developed protocol features wide substrate scope (nearly 80 examples), broad functional group tolerance, and potential for the late‐stage functionalization of bioactive compounds. The isolation and crystallographic analysis of a catalytically competent π‐allyl Pd complex suggests that the pathway leading to the allylic products proceeds through a different manifold as previously proposed for the functionalization of VECs with nucleophiles.