Abstract
Investigations revealed that N-Benzyl-N-(2-methoxyphenyl)cyclo-hex-1-enecarboxamide did not photocyclize in the solid state. The methoxy group was involved in intermolecular steric interactions and so prevented the rotation of the N-phenyl group in the crystal. N-Benzyl-N-(2-methoxyphenyl)cyclo-hex-1-enecarboxamide was prepared under a study on photocyclization of enamides and thioamides in the solid state and crystals were grown from a hexane solution.
Original language | English |
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Pages (from-to) | e151 |
Journal | Acta Crystallographica Section C: Crystal Structure Communications |
Volume | 56 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2000 Jan 1 |
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)