Literature DB >> 25407375

One-pot quadruple/triple reaction sequence: a useful tool for the synthesis of natural products.

K Kashinath1, D Srinivasa Reddy.   

Abstract

Multiple reactions in one pot has always been a useful technique for synthetic organic chemists, as it can minimizes solvent usage, time and the number of purification steps when compared to individual multi-step syntheses. In line with this, here in this perspective we discuss a one-pot quadruple/triple reaction sequence comprising an enyne ring-closing metathesis/cross-metathesis/Diels-Alder/aromatization for the synthesis of natural products setting.

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Year:  2014        PMID: 25407375     DOI: 10.1039/c4ob02143f

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


  3 in total

1.  Modular Synthesis of Novel Macrocycles Bearing α,β-Unsaturated Chemotypes through a Series of One-Pot, Sequential Protocols.

Authors:  Salim Javed; Mahipal Bodugam; Jessica Torres; Arghya Ganguly; Paul R Hanson
Journal:  Chemistry       Date:  2016-04-05       Impact factor: 5.236

2.  A Pot-Economical Approach to the Total Synthesis of Sch-725674.

Authors:  Mahipal Bodugam; Salim Javed; Arghya Ganguly; Jessica Torres; Paul R Hanson
Journal:  Org Lett       Date:  2016-01-13       Impact factor: 6.005

3.  Synthesis of highly substituted benzene ring systems through three-component coupling of enyne imines, Fischer carbene complexes, and electron-deficient alkynes.

Authors:  Bishnu Dhakal; Lalith S R Gamage; Yanshi Zhang; James W Herndon
Journal:  Tetrahedron Lett       Date:  2017-02-24       Impact factor: 2.415

  3 in total

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