Literature DB >> 26940980

Silver catalyzed domino aza-annulation/Diels-Alder cyclization of 2-ene-yne anilines: a facile one-pot access to carbazole, dihydrocarbazole and tetrahydrocarbazole frameworks.

Namballa Hari Krishna1, A Prasanth Saraswati2, Manda Sathish3, Nagula Shankaraiah2, Ahmed Kamal1.   

Abstract

An unprecedented and efficient AgSbF6-catalyzed domino aza-annulation/Diels-Alder/aromatization cascade for the construction of carbazoles, dihydrocarbazoles and tetrahydrocarbazoles was achieved using 2-(but-3-en-1-yn-1-yl) anilines in the presence of suitable dienophiles. The reaction proceeds via the in situ generation of 2-vinyl indoles and their subsequent trapping by various dienophiles with concomitant aromatization. A series of symmetrical, unsymmetrical and base sensitive dienophiles provide the corresponding carbazoles under mild conditions in excellent yields with high regioselectivity.

Entities:  

Year:  2016        PMID: 26940980     DOI: 10.1039/c6cc00633g

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


  1 in total

1.  Ring-opening cyclization of activated spiro-aziridine oxindoles with heteroarenes: a facile synthetic approach to spiro-oxindole-fused pyrroloindolines.

Authors:  Sonal Bhandari; Sravani Sana; Vandana Lahoti; Ramya Tokala; Nagula Shankaraiah
Journal:  RSC Adv       Date:  2020-04-24       Impact factor: 4.036

  1 in total

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