Literature DB >> 31180229

Weak Coordinating Carboxylate Directed Rhodium(III)-Catalyzed C-H Activation: Switchable Decarboxylative Heck-Type and [4 + 1] Annulation Reactions with Maleimides.

Mahadev Sharanappa Sherikar1, Kandikere Ramaiah Prabhu1.   

Abstract

A weakly coordinating carboxylate directing group assisted C-H activation with maleimides leading to novel and switchable decarboxylative Heck-type and [4 + 1] annulation products catalyzed by Rh(III) has been reported. In these reactions, solvents play a vital role in switching the selectivity. An aprotic solvent, THF, leads to the decarboxylative Heck-type product while the protic solvent, TFE, results in the [4 + 1] annulation product. The methodology shows high functional group tolerance.

Entities:  

Year:  2019        PMID: 31180229     DOI: 10.1021/acs.orglett.9b01412

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Preparation of cyclic imides from alkene-tethered amides: application of homogeneous Cu(ii) catalytic systems.

Authors:  Zhenghui Liu; Peng Wang; Hualin Ou; Zhenzhong Yan; Suqing Chen; Xingxing Tan; Dongkun Yu; Xinhui Zhao; Tiancheng Mu
Journal:  RSC Adv       Date:  2020-02-21       Impact factor: 4.036

2.  Synthesis of Succinimide-Linked Indazol-3-ols Derived from Maleimides under Rh(III) Catalysis.

Authors:  Ju Young Kang; Suho Kim; Junghyea Moon; Eunjae Chung; Jaeyoung Kim; So Young Kyung; Hyung Sik Kim; Neeraj Kumar Mishra; In Su Kim
Journal:  ACS Omega       Date:  2022-04-21
  2 in total

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