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I2-Catalyzed transformation of o-aminobenzamide to o-ureidobenzonitrile using isothiocyanates.
Shamanth, Sadashivamurthy; Chaithra, Nagaraju; Gurukiran, Mahesha; Mamatha, Mahesha; Lokanath, N K; Rangappa, Kanchugarakoppal S; Mantelingu, Kempegowda.
Afiliação
  • Shamanth S; DOS in Chemistry, Manasagangotri, University of Mysore, Mysuru-570006, Karnataka, India. kmlingu@gmail.com rangappaks@gmail.com.
  • Chaithra N; DOS in Chemistry, Manasagangotri, University of Mysore, Mysuru-570006, Karnataka, India. kmlingu@gmail.com rangappaks@gmail.com.
  • Gurukiran M; DOS in Chemistry, Manasagangotri, University of Mysore, Mysuru-570006, Karnataka, India. kmlingu@gmail.com rangappaks@gmail.com.
  • Mamatha M; SRSMNGFG College, Barkur-576210, Udupi Dist., Karnataka, India.
  • Lokanath NK; DOS in Physics, Manasagangotri, University of Mysore, Mysuru-570006, India.
  • Rangappa KS; DOS in Chemistry, Manasagangotri, University of Mysore, Mysuru-570006, Karnataka, India. kmlingu@gmail.com rangappaks@gmail.com.
  • Mantelingu K; DOS in Chemistry, Manasagangotri, University of Mysore, Mysuru-570006, Karnataka, India. kmlingu@gmail.com rangappaks@gmail.com.
Org Biomol Chem ; 18(14): 2678-2684, 2020 04 08.
Article em En | MEDLINE | ID: mdl-32202293
ABSTRACT
The present work describes an unexpected and unique protocol for the iodine catalysed synthesis of o-ureidobenzonitriles using o-aminobenzamides and isothiocyanates via intramolecular rearrangement. The metal-free route achieved here is insensitive to moisture and applicable to the synthesis of a wide variety of o-ureidobenzonitriles with excellent yields even in a scalable fashion.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2020 Tipo de documento: Article