Literature DB >> 16832514

A novel synthesis of beta-lactam fused cyclic enediynes by intramolecular Kinugasa reaction.

Runa Pal1, Amit Basak.   

Abstract

A general synthetic route to beta-lactam-fused enediynes by intramolecular Kinugasa reaction has been successfully developed. The method has widened the scope of Kinugasa reaction in the synthesis of sensitive systems like the one described in this communication.

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Year:  2006        PMID： 16832514     DOI： 10.1039/b605743h

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


  2 in total

1.  A highly stereoselective synthesis of chiral alpha-amino-beta-lactams via the Kinugasa reaction employing ynamides.

Authors:  Xuejun Zhang; Richard P Hsung; Hongyan Li; Yu Zhang; Whitney L Johnson; Ruth Figueroa
Journal:  Org Lett       Date:  2008-07-10       Impact factor: 6.005

2.  Synthesis of 1,3-diaryl-spiro[azetidine-2,3'-indoline]-2',4-diones via the Staudinger reaction: cis- or trans-diastereoselectivity with different addition modes.

Authors:  Vadim Filatov; Maksim Kukushkin; Juliana Kuznetsova; Dmitry Skvortsov; Viktor Tafeenko; Nikolay Zyk; Alexander Majouga; Elena Beloglazkina
Journal:  RSC Adv       Date:  2020-04-06       Impact factor: 4.036
  2 in total

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