Literature DB >> 27286137

Pd-catalyzed one-pot sequential unsymmetrical cross-coupling reactions of aryl/heteroaryl 1,2-dihalides.

Abhinandan K Danodia1, Rakesh K Saunthwal1, Monika Patel1, Rakesh K Tiwari2, Akhilesh K Verma1.   

Abstract

Efficient, step-economic, Pd(ii)-catalyzed one-pot sequential Sonogashira/Sonogashira, Sonogashira/Suzuki, Sonogashira/Heck, Suzuki/Sonogashira, Suzuki/Suzuki, Suzuki/Heck, Heck/Sonogashira, Heck/Suzuki and Heck/Heck cross coupling reactions of sterically hindered aryl/heteroaryl 1,2-dihalides have been developed. The present methodology allows the conversion of easily available aryl/heteroaryl 1,2-dihalides into synthetically useful unsymmetrically substituted arenes/heteroarenes in good to excellent yields under mild reaction conditions. This methodology is a powerful tool for building a versatile substrate which can be utilized for the synthesis of various organic scaffolds.

Entities:  

Year:  2016        PMID: 27286137     DOI: 10.1039/c6ob01049k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Palladium-catalyzed highly regioselective mono and double Sonogashira cross-coupling reactions of 5-substituted-1,2,3-triiodobenzene under ambient conditions.

Authors:  Raed M Al-Zoubi; Mothana K Al-Omari; Walid K Al-Jammal; Michael J Ferguson
Journal:  RSC Adv       Date:  2020-04-24       Impact factor: 3.361

  1 in total

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