Literature DB >> 23694954

Palladium-catalysed aerobic oxidative Heck-type alkenylation of Csp3-H for pyrrole synthesis.

Lingkui Meng1, Kun Wu, Chao Liu, Aiwen Lei.   

Abstract

The first palladium-catalysed aerobic oxidative intramolecular alkenylation of Csp(3)-H bonds was described. The reaction conditions were mild and molecular oxygen was used as the terminal oxidant. Kinetic studies showed that the Csp(3)-H metallation step was a slow step.

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Year:  2013        PMID: 23694954     DOI: 10.1039/c3cc42307g

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


  2 in total

1.  A chemoselective route to β-enamino esters and thioesters.

Authors:  Dongyue Xin; Kevin Burgess
Journal:  Org Lett       Date:  2014-03-31       Impact factor: 6.005

2.  One-pot sequential multicomponent reaction between in situ generated aldimines and succinaldehyde: facile synthesis of substituted pyrrole-3-carbaldehydes and applications towards medicinally important fused heterocycles.

Authors:  Anoop Singh; Nisar A Mir; Sachin Choudhary; Deepika Singh; Preetika Sharma; Rajni Kant; Indresh Kumar
Journal:  RSC Adv       Date:  2018-04-24       Impact factor: 4.036

  2 in total

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