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Literature DB >> 12123011

Catalytic and highly regiospecific carbon-carbon bond formation at alpha-position of Michael acceptor by palladium complex.

Jae-Goo Shim¹, Jong Chul Park, Chan Sik Cho, Sang Chul Shim, Yoshinori Yamamoto.

Abstract

Activated olefins react with allyl acetates and Bu3SnH in the presence of a catalytic amount of a palladium catalyst to afford the corresponding products which construct a new C-C bond selectively at the alpha-position of Michael acceptors.

Entities: Chemical

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Year: 2002 PMID： 12123011 DOI： 10.1039/b201545p

Source DB: PubMed Journal: Chem Commun (Camb) ISSN： 1359-7345 Impact factor: 6.222

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Cited

1 in total

1. Highly Regioselective Synthesis of Oxindolyl-Pyrroles and Quinolines via a One-Pot, Sequential Meyer-Schuster Rearrangement, Anti-Michael Addition/C_(sp³)-H Functionalization, and Azacyclization.

Authors: Srinivasarao Yaragorla; Ravikrishna Dada; P Rajesh; Manju Sharma
Journal: ACS Omega Date: 2018-03-09

1 in total

Catalytic and highly regiospecific carbon-carbon bond formation at alpha-position of Michael acceptor by palladium complex.

1. Highly Regioselective Synthesis of Oxindolyl-Pyrroles and Quinolines via a One-Pot, Sequential Meyer-Schuster Rearrangement, Anti-Michael Addition/C(sp3)-H Functionalization, and Azacyclization.

1. Highly Regioselective Synthesis of Oxindolyl-Pyrroles and Quinolines via a One-Pot, Sequential Meyer-Schuster Rearrangement, Anti-Michael Addition/C_(sp³)-H Functionalization, and Azacyclization.