1997
DOI: 10.1002/chin.199734198
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ChemInform Abstract: 1,3‐Thiazepines. Part 4. Reaction of 2‐Iminothiazepines with Methyl Acrylate. Crystal and Molecular Structure of 2‐Phenylimino‐3‐(β‐ methoxycarbonylethyl)‐ and 2‐Benzyliminohexahydro‐1,3‐thiazepines.

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“…1,3-Thiazepines are studied less than their fiveor six-membered analogs. A series of hydrogenated 1,3thiazepine derivatives have been obtained by Ambartsumova et al [7][8][9][10]], including 2-benzyliminohexahydro-1,3-thiazepine (imine form), which was reported as an amine form (2-benzyl aminotetrahydro-1,3-thiazepine) by Olszenko-Piontkowa and Urbanski [11]. The single-crystal X-ray diffraction method plays an important role to attribute a reaction product to an imine form [8].…”
Section: Introductionmentioning
confidence: 99%
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“…1,3-Thiazepines are studied less than their fiveor six-membered analogs. A series of hydrogenated 1,3thiazepine derivatives have been obtained by Ambartsumova et al [7][8][9][10]], including 2-benzyliminohexahydro-1,3-thiazepine (imine form), which was reported as an amine form (2-benzyl aminotetrahydro-1,3-thiazepine) by Olszenko-Piontkowa and Urbanski [11]. The single-crystal X-ray diffraction method plays an important role to attribute a reaction product to an imine form [8].…”
Section: Introductionmentioning
confidence: 99%
“…A series of hydrogenated 1,3thiazepine derivatives have been obtained by Ambartsumova et al [7][8][9][10]], including 2-benzyliminohexahydro-1,3-thiazepine (imine form), which was reported as an amine form (2-benzyl aminotetrahydro-1,3-thiazepine) by Olszenko-Piontkowa and Urbanski [11]. The single-crystal X-ray diffraction method plays an important role to attribute a reaction product to an imine form [8]. Furthermore, the spatial arrangement of the atoms and the conformation of the seven-membered ring, which was obtained by X-ray diffraction analysis [8] or theoretical methods [12], is of great importance for amine-imine tautomeric chemistry.…”
Section: Introductionmentioning
confidence: 99%
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