Literature DB >> 9871665

Synthesis of constrained alpha-amino acid derivatives via ring-closing olefin metathesis.

S Kotha1, N Sreenivasachary.   

Abstract

Five and seven membered constrained alpha-amino acid derivatives were synthesized using ring-closing metathesis reaction as a key step.

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Year:  1998        PMID： 9871665     DOI： 10.1016/s0960-894x(98)00002-x

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN： 0960-894X            Impact factor:   2.823


  4 in total

1.  A new constrained proline analogue with an 8-azabicyclo[3.2.1]octane skeleton.

Authors:  Diego Casabona; Ana I Jiménez; Carlos Cativiela
Journal:  Tetrahedron       Date:  2007-06-04       Impact factor: 2.457

2.  Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines.

Authors:  Sergiy V Chepyshev; J Armando Lujan-Montelongo; Allen Chao; Fraser F Fleming
Journal:  Angew Chem Int Ed Engl       Date:  2017-03-13       Impact factor: 15.336

3.  Alkyl Sulfinates: Formal Nucleophiles for Synthesizing TosMIC Analogs.

Authors:  J Armando Lujan-Montelongo; Angel Ojeda Estevez; Fraser F Fleming
Journal:  European J Org Chem       Date:  2015-03

4.  Design and synthesis of hybrid cyclophanes containing thiophene and indole units via Grignard reaction, Fischer indolization and ring-closing metathesis as key steps.

Authors:  Ajay Kumar Chinnam; Mukesh Eknathrao Shirbhate; Sambasivarao Kotha
Journal:  Beilstein J Org Chem       Date:  2015-08-31       Impact factor: 2.883
  4 in total

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