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In the title compound, C14H24ClNO, the bond lengths and angles are within normal ranges and comparable to those of related compounds. The geometry of the two cyclohexyl groups is the normal chair conformation. The crystal packing is stabilized by CH⋯C short-contact interactions. [ABSTRACT FROM AUTHOR]

In the mol­ecule of the title compound, C24H17Cl2N3O2S, the mean plane of the tricyclic thienopyridopyrimidine system is roughly orthogonal to both benzene planes, the dihedral angles being 107.8 (1) and 99.6 (1)° for the benzene planes in the p-chloro­phen­oxy and p-chloro­phenyl groups, respectively. The dihedral angle formed by the two benzene rings is 101.4 (1)°. [ABSTRACT FROM AUTHOR]

The asymmetric unit of the title compound, C23H23ClN4OS, contains two crystallographically independent mol­ecules in which the orientations of the propyl­amine group and chloro­phenyl rings with respect to the fused ring system are different. The terminal cyclo­hexene ring adopts a half-chair conformation. The crystal packing is stabilized by N—H⋯O, N—H⋯N and C—H⋯O hydrogen bonds and π–π inter­actions. [ABSTRACT FROM AUTHOR]

The title compound, C17H16N4O2, a potent fungicidal agent, has been synthesized and its crystal structure determined. The dihedral angles between the planes of the pyridinyl and triazole rings, and between the substituted phenyl and triazole rings are 82.7 (2)° and 77.0 (3)°, respectively. [ABSTRACT FROM AUTHOR]

The title compound, C11H7C12N5S, has been synthesized as a potent fungicidal agent and its crystal structure was determined. In the crystal structure there are weak intermolecular N—H⋯N hydrogen bonds. The dihedral angles between the planes of the thia­zole and triazole rings and between the substituted phenyl and thia­zole rings are 36.3 (2) and 47.1 (3)°, respectively. [ABSTRACT FROM AUTHOR]

The title compound, C14H13N3O3S, has been synthesized as a potent fungicidal agent. The 1,3-thiazolidine ring is approximately planar and makes a dihedral angle of 84.9 (2)° with the phenyl ring. There are weak intramolecular C—H...O and C—H...N hydrogen bonds, which stabilize the molecular structure. [ABSTRACT FROM AUTHOR]

The title compound, C26H36O5, is a derivative of abietic acid formed by an endo-Diels–Alder reaction between maleic anhydride and the diene levopimaric acid ethyl ester. The two fused and unbridged cyclohexane rings have chair conformations and the anhydride ring is planar. [ABSTRACT FROM AUTHOR]