Your browser doesn't support javascript.
loading
Synthesis of Benzo[e][1,4,3]oxathiazin-3-one 1-Oxides from NH-S-(2-Hydroxyaryl)sulfoximines.
Periasamy, Kiruthika; van Bonn, Pit; Orloff, Runa Tschekorsky; Völcker, Nils; Lu, Qiulan; Rissanen, Kari; Bolm, Carsten.
Afiliação
  • Periasamy K; Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany.
  • van Bonn P; Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany.
  • Orloff RT; Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany.
  • Völcker N; Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany.
  • Lu Q; Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany.
  • Rissanen K; University of Jyvaskyla, Department of Chemistry, Survontie 9 B, P.O. Box 35, 40014 Jyväskylä, Finland.
  • Bolm C; Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany.
J Org Chem ; 89(11): 8286-8290, 2024 Jun 07.
Article em En | MEDLINE | ID: mdl-38743919
ABSTRACT
Cyclizations of NH-S-(2-hydroxyaryl)sulfoximines with 1,1'-carbonyldiimidazol (CDI) give unprecedented benzo[e][1,4,3]oxathiazin-3-one 1-oxides in good yields. The standard synthetic protocol involves the use of DCE at an increased temperature for 16 h. Under mechanochemical conditions, a representative product was obtained without a solvent at ambient temperature in only 60 min. X-ray single-crystal structure analysis confirmed the molecular scaffold representing a three-dimensional heterocycle.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article