A 1: 1 Adduct of 2‐Aminobenzothiazole and a Urea Derivative, and Its Spatial Arrangement

Matthew G. Davidson, Avelino Martin, Paul R. Raithby, Ronald Snaith, David R. Armstrong, Dietmar Stalke

Research output: Contribution to journalArticlepeer-review

Abstract

A central tunnel catches the eye in the symmetric arrangement of the adduct (1 · 2)2 of 2‐aminobenzothiazole 1, an analogue of a DNA base, and 1,3‐dimethyl‐2‐oxohexahy‐dropyrimidine (2) (on the right a view down the b axis). The adduct is dimeric; two molecules of 1 form a base pair, and each molecule of 1 is also bound to one molecule of 2. The halves of the dimer are linked by hydrogen bonds, but each dimer is discrete. (Figure Presented.)

Original languageEnglish
Pages (from-to)1634-1636
Number of pages3
JournalAngewandte Chemie International Edition in English
Volume31
Issue number12
DOIs
Publication statusPublished - 31 Dec 1992

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry

Fingerprint

Dive into the research topics of 'A 1: 1 Adduct of 2‐Aminobenzothiazole and a Urea Derivative, and Its Spatial Arrangement'. Together they form a unique fingerprint.

Cite this