Your browser doesn't support javascript.
loading
Facile synthesis of 1-alkoxy-1H-benzo- and 7-azabenzotriazoles from peptide coupling agents, mechanistic studies, and synthetic applications.
Lakshman, Mahesh K; Singh, Manish K; Kumar, Mukesh; Chamala, Raghu Ram; Yedulla, Vijayender R; Wagner, Domenick; Leung, Evan; Yang, Lijia; Matin, Asha; Ahmad, Sadia.
Afiliação
  • Lakshman MK; Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, NY 10031, USA.
  • Singh MK; Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, NY 10031, USA.
  • Kumar M; Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, NY 10031, USA.
  • Chamala RR; Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, NY 10031, USA.
  • Yedulla VR; Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, NY 10031, USA.
  • Wagner D; Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, NY 10031, USA.
  • Leung E; Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, NY 10031, USA.
  • Yang L; Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, NY 10031, USA.
  • Matin A; Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, NY 10031, USA.
  • Ahmad S; Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, NY 10031, USA.
Beilstein J Org Chem ; 10: 1919-32, 2014.
Article em En | MEDLINE | ID: mdl-25246951

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Beilstein J Org Chem Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Beilstein J Org Chem Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos