Literature DB >> 17315882

A new versatile strategy for C-aryl glycosides.

Krishna P Kaliappan1, Ayyagari V Subrahmanyam.   

Abstract

A versatile strategy involving a sequential intermolecular enyne metathesis of C-alkynyl glycosides with ethylene, Diels-Alder, and aromatization reactions is successfully developed to provide a range of C-aryl glycosides. [reaction: see text]

Entities:  

Year:  2007        PMID： 17315882     DOI： 10.1021/ol0701159

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


  4 in total

1.  Ene-yne cross-metathesis with ruthenium carbene catalysts.

Authors:  Cédric Fischmeister; Christian Bruneau
Journal:  Beilstein J Org Chem       Date:  2011-02-04       Impact factor: 2.883

2.  Tandem cross enyne metathesis (CEYM)-intramolecular Diels-Alder reaction (IMDAR). An easy entry to linear bicyclic scaffolds.

Authors:  Javier Miró; María Sánchez-Roselló; Álvaro Sanz; Fernando Rabasa; Carlos Del Pozo; Santos Fustero
Journal:  Beilstein J Org Chem       Date:  2015-08-25       Impact factor: 2.883

3.  Design and efficient synthesis of pyrazoline and isoxazole bridged indole C-glycoside hybrids as potential anticancer agents.

Authors:  Priti Kumari; Vishnu S Mishra; Chintam Narayana; Ashish Khanna; Anindita Chakrabarty; Ram Sagar
Journal:  Sci Rep       Date:  2020-04-20       Impact factor: 4.379

Review 4.  A new and informative [a,b,c,d] nomenclature for one-pot multistep transformations: a simple tool to measure synthetic efficiency.

Authors:  Satrajit Indu; Krishna P Kaliappan
Journal:  RSC Adv       Date:  2018-06-11       Impact factor: 4.036
  4 in total

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