Literature DB >> 21956237

Synthetic applications of the nickel-catalyzed cyclization of alkynes combined with addition reactions in a domino process.

Muriel Durandetti1, Lucie Hardou, Rudy Lhermet, Mathieu Rouen, Jacques Maddaluno.   

Abstract

Carbonickelations of alkynes and functionalization of the resulting vinylnickel moiety have been performed efficiently in a nickel-catalyzed domino cyclization-condensation process. This reaction, which does not require the preparation of any other organometallic reagent, proceeds only by exo-dig cyclization. This convenient and mild method constitutes a one-pot synthesis of substituted dihydrobenzofurans, chromans, isochromans, indoles, or indanes. Theses valuable products are generally obtained in good yields and high stereoselectivity. They are shown to be useful synthons for rapid access to functionalized polycyclic skeletons.
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Year:  2011        PMID: 21956237     DOI: 10.1002/chem.201100967

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Intramolecular carbonickelation of alkenes.

Authors:  Rudy Lhermet; Muriel Durandetti; Jacques Maddaluno
Journal:  Beilstein J Org Chem       Date:  2013-04-12       Impact factor: 2.883

2.  Palladium-Catalyzed Synthesis of 2,3-Disubstituted Benzofurans: An Approach Towards the Synthesis of Deuterium Labeled Compounds.

Authors:  Soumitra Agasti; Soham Maity; Kalman J Szabo; Debabrata Maiti
Journal:  Adv Synth Catal       Date:  2015-07-14       Impact factor: 5.837

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.