Chemical Transformations of Tetracyclo[3.3.1.13,7.01,3]decane (1,3-Dehydroadamantane): VI. Reactions of 1,3-Dehydroadamantane with Carboxylic Acid Chlorides
- 作者: Mokhov V.M.1, Butov G.M.2, Saad K.R.2
- 
							隶属关系: 
							- Volgograd State Technical University
- Volzhsky Polytechnic Institute (Branch)
 
- 期: 卷 54, 编号 6 (2018)
- 页面: 840-843
- 栏目: Article
- URL: https://journals.rcsi.science/1070-4280/article/view/218039
- DOI: https://doi.org/10.1134/S1070428018060039
- ID: 218039
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详细
1,3-Dehydroadamantane reacted with saturated carboxylic acid chlorides to give the corresponding 1-acyl-3-chloroadmantanes as the major products. In some cases, minor products of insertion into the Cα–H bond of acyl chloride were formed. The reactions of 1,3-dehydroadamantane with aromatic (heteroaromatic) carboxylic acid chlorides selectively afforded aryl (hetaryl) 3-chloroadamantan-1-yl ketones. The described reactions provide a synthetic route to difficultly accessible alkyl (aryl) ketones containing a 3-chloroadamantan- 1-yl group in one step under mild conditions with high yields.
作者简介
V. Mokhov
Volgograd State Technical University
														Email: butov@volpi.ru
				                					                																			                												                	俄罗斯联邦, 							pr. imeni Lenina 28, Volgograd, 400005						
G. Butov
Volzhsky Polytechnic Institute (Branch)
							编辑信件的主要联系方式.
							Email: butov@volpi.ru
				                					                																			                												                	俄罗斯联邦, 							ul. Engel’sa 42a, Volzhsky, Volgograd oblast, 404121						
K. Saad
Volzhsky Polytechnic Institute (Branch)
														Email: butov@volpi.ru
				                					                																			                												                	俄罗斯联邦, 							ul. Engel’sa 42a, Volzhsky, Volgograd oblast, 404121						
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