Some special features of hydroalumination-iodination of alkyne-1, 4-diols
…, GM Makaryan, MR Hovhannisyan, FS Kinoyan…
Index: Gharibyan; Makaryan; Hovhannisyan; Kinoyan; Chobanyan Russian Journal of General Chemistry, 2014 , vol. 84, # 3 p. 457 - 464 Zh. Obshch. Khim., 2014 , vol. 84, # 3 p. 399 - 406,8
Full Text: HTML
Citation Number: 0
Abstract
Abstract Hydroalumination-iodination of alkyne-1, 4-diols of different structure showed that with increasing number of substituents at the C-OH group the amount of β-iodo-substituted products with respect to this group increased. In the case of symmetric secondary 1, 4-diols the reaction results in a 1: 1 mixture of stereoisomeric iodoalkenediols, and in the case of phenyl substituents the reaction proceeds regio-and stereoselectively to give an ...
Related Articles:
[Grigorjeva, Liene; Jirgensons, Aigars European Journal of Organic Chemistry, 2011 , # 13 p. 2421 - 2425]
[Hazra, Chinmoy K.; Irran, Elisabeth; Oestreich, Martin European Journal of Organic Chemistry, 2013 , # 22 p. 4903 - 4908]
[Duffy, Michael G.; Grayson, David H. Journal of the Chemical Society. Perkin Transactions 1, 2002 , # 13 p. 1555 - 1563]
[Murakami, Hiromi; Minami, Tatsuya; Ozawa, Fumiyuki Journal of Organic Chemistry, 2004 , vol. 69, # 13 p. 4482 - 4486]
A total synthesis of dl-cerulenin
[Boeckman Jr.; Thomas Journal of the American Chemical Society, 1979 , vol. 101, # 4 p. 987 - 994]