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Updated: May 27, 2026

Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
1,3-Dicyclo-hexyl-3-[(pyridin-2-yl)carbon-yl]urea monohydrate from synchrotron radiation
Abstract:
The title urea derivative crystallizes as a monohydrate, C(19)H(27)N(3)O(2)·H(2)O. The central C(3)N grouping is almost planar (r.m.s. deviation = 0.0092 Å), and the amide and pyridine groups are substanti-ally twisted out this plane [dihedral angles = 62.80 (12) and 34.98 (10)°, respectively]. Supra-molecular double chains propagating along the b-axis direction feature in the crystal packing whereby linear chains sustained by N-H⋯O hydrogen bonds formed between the amide groups are linked by helical chains of water mol-ecules (linked by O-H⋯O hydrogen bonds). The H atom that participates in these water chains is disordered over two positions of equal occupancy. The double chains are connected into a two-dimensional array by C-H⋯O contacts and the layers stack along the a axis.
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