Literature DB >> 27709960

Ag(I)-Catalyzed Domino Cyclization-Addition Sequence with Simultaneous Carbonyl and Alkyne Activation as a Route to 2,2'-Disubstituted Bisindolylarylmethanes.

Swastik Karmakar1, Prasanta Das1, Debjyoti Ray1, Subhankar Ghosh2, Shital K Chattopadhyay2.   

Abstract

An efficient synthesis of symmetrical 3, 3'-bisindolylarylmethanes with various substituents on the indole moiety has been developed by Ag(I)-catalyzed cycloisomerization and an deoxygenative addition sequence on o-alkynylanilines and aryl aldehydes. Ag(I) is proposed to activate alkyne unit and carbonyl moiety simultaneously leading to a domino first 5-endo-dig indole annulation, addition to C═O, second indole annulation, and its dehydroxylative addition.

Entities:  

Year:  2016        PMID: 27709960     DOI: 10.1021/acs.orglett.6b02321

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


  2 in total

1.  Bis-indolylation of aldehydes and ketones using silica-supported FeCl3: molecular docking studies of bisindoles by targeting SARS-CoV-2 main protease binding sites.

Authors:  Barnali Deb; Sudhan Debnath; Ankita Chakraborty; Swapan Majumdar
Journal:  RSC Adv       Date:  2021-09-16       Impact factor: 4.036

2.  A copper(ii)-catalyzed annulative formylation of o-alkynylanilines with DMF: a single-step strategy for 3-formyl indoles.

Authors:  Balaji Ganesan; Gopal Chandru Senadi; Bing-Chun Guo; Min-Yuan Hung; Wei-Yu Lin
Journal:  RSC Adv       Date:  2018-12-07       Impact factor: 3.361

  2 in total

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