Synthesis and steric structure of N鈥?(arylmethylidene)-N鈥斥€?(1-methyl-3-phenylprop-2-yn-1-ylidene)thiocarbonohydrazides
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- 作者：T. E. Glotova (1)
M. Yu. Dvorko (1)
N. N. Chipanina (1)
A. I. Albanov (1)
L. V. Sherstyannikova (1)
O. N. Kazheva (2)
A. N. Chekhlov (2)
O. A. D鈥檡achenko (2) - 刊名：Russian Journal of Organic Chemistry
- 出版年：2008
- 出版时间：January 2008
- 年：2008
- 卷：44
- 期：1
- 页码：114-119
- 全文大小：364KB
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23. Sheldrick, G.M., / SHELXL-97. A Program for the Refinement of Crystal Structures. Gottingen: Univ. of Gottingen, 1997. - 作者单位：T. E. Glotova (1)
M. Yu. Dvorko (1)
N. N. Chipanina (1)
A. I. Albanov (1)
L. V. Sherstyannikova (1)
O. N. Kazheva (2)
A. N. Chekhlov (2)
O. A. D鈥檡achenko (2)
1. Favorskii Irkutsk Institute of Chemistry, Siberian Division, Russian Academy of Sciences, ul. Favorskogo 1, Irkutsk, 664033, Russia
2. Institute of Chemical Physics Problems, Russian Academy of Sciences, Chernogolovka, Moscow oblast, Russia - ISSN：1608-3393
文摘
Thiocarbonohydrazones derived from aromatic aldehydes reacted with 4-phenylbut-3-yn-2-one in aqueous acetic acid (20掳C, 2 h) to produce previously unknown N鈥?[(E-s-cis)-arylmethylidene]-N鈥斥€?[(Z-s-trans)-1-methyl-3-phenylprop-2-yn-1-ylidene]thiocarbonohydrazides with high chemo-, regio-, and stereoselectivity. The steric structure of N鈥?[(E-s-cis)-benzylidene]-N鈥斥€?[(Z-s-trans)-1-methyl-3-phenylprop-2-yn-1-ylidene]thiocarbonohydrazide in crystal and in solution was studied by X-ray analysis and IR and NMR spectroscopy.