610299-84-8

Upstream product

• 911207-06-2 C₂₁⁽²⁾H₁₄H₉ON 
• 36278-22-5 1-cyclohexenoyl chloride 
• 167750-79-0 α,α,2,3,4,5,6-heptadeuterobenzylamine 
• 17901-93-8 benzaldehyde-d6 
• 636-82-8 cyclohexene-1-carboxylic acid 
• 911207-05-1 C₁₄⁽²⁾H₁₅N 

Relevant academic research and scientific papers

Neutron diffraction analysis of deuterium transfer in chiral β-thiolactam formation in the crystalline state

Since N,N-dibenzyl-1-cyclohexenecarbothioamide is photoisomerized to the optically active β-thiolactam with the retention of the single-crystal form, the mechanism of chirality induction was identified by X-ray crystal structure analyses during the process of the reaction [Hosoya et al. (2002). Bull. Chem. Soc. Jpn, 75, 2147-2151]. In order to clarify the mechanism of hydrogen transfer in the reaction, the H atoms of the benzyl groups were replaced with deuterium atoms. The crystal structure after photoisomerization was analyzed by neutron diffraction. One of four deuterium atoms of the two benzyl groups is transferred to the C atom of the cyclohexene ring. The absolute configuration of the -C*HD- group (chiral methylene) in the photoproduct β-thiolactam revealed that the deuterium atom occupies the equatorial position. This suggests that the deuterium atom is not transferred from the benzyl group of a neighbouring molecule, but from one of the benzyl groups within the molecule.