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

doi:10.1002/anie.199216341

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 journal › Article › peer-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 language	English
Pages (from-to)	1634-1636
Number of pages	3
Journal	Angewandte Chemie International Edition in English
Volume	31
Issue number	12
DOIs	https://doi.org/10.1002/anie.199216341
Publication status	Published - 31 Dec 1992

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Catalysis
General Chemistry

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

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.)",

author = "Davidson, \{Matthew G.\} and Avelino Martin and Raithby, \{Paul R.\} and Ronald Snaith and Armstrong, \{David R.\} and Dietmar Stalke",

year = "1992",

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day = "31",

doi = "10.1002/anie.199216341",

language = "English",

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T2 - 1 Adduct of 2‐Aminobenzothiazole and a Urea Derivative, and Its Spatial Arrangement

AU - Davidson, Matthew G.

AU - Martin, Avelino

AU - Raithby, Paul R.

AU - Snaith, Ronald

AU - Armstrong, David R.

AU - Stalke, Dietmar

PY - 1992/12/31

Y1 - 1992/12/31

N2 - 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.)

AB - 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.)

UR - https://www.scopus.com/pages/publications/33748220944

U2 - 10.1002/anie.199216341

DO - 10.1002/anie.199216341

M3 - Article

AN - SCOPUS:33748220944

SN - 0570-0833

VL - 31

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JO - Angewandte Chemie International Edition in English

JF - Angewandte Chemie International Edition in English

IS - 12

ER -

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

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