Reductive coupling of alkynes by oxobis (diethyldithiocarbamato) molybdenum (IV)–sodium borohydride
…, D Lloyd-Jones, GSK Kannangara, AT Baker
Index: Conn; Lloyd-Jones; Kannangara; Baker Journal of Organometallic Chemistry, 1999 , vol. 585, # 1 p. 134 - 140
Full Text: HTML
Citation Number: 2
Abstract
The reductive coupling of terminal alkynes and the intramolecular cyclization of diynes by oxobis (diethyldithiocarbamato) molybdenum (IV) in the presence of sodium borohydride are reported. The reaction leads to a mixture of products resulting primarily from 'head to tail'coupling of the alkynes. 1, 7-Octadiyne undergoes cyclization to afford cycloheptene-3- ylidene in 45% yield. The product distribution appears to be controlled by steric factors ...
Related Articles:
[Peng, Jianbiao; Liu, Xiang; Kishi, Yoshito Tetrahedron Letters, 2011 , vol. 52, # 17 p. 2172 - 2175]
[Peng, Jianbiao; Liu, Xiang; Kishi, Yoshito Tetrahedron Letters, 2011 , vol. 52, # 17 p. 2172 - 2175]
[Peng, Jianbiao; Liu, Xiang; Kishi, Yoshito Tetrahedron Letters, 2011 , vol. 52, # 17 p. 2172 - 2175]
[Peng, Jianbiao; Liu, Xiang; Kishi, Yoshito Tetrahedron Letters, 2011 , vol. 52, # 17 p. 2172 - 2175]
[Chernichenko, Konstantin; Madarasz, Adam; Papai, Imre; Nieger, Martin; Leskelae, Markku; Repo, Timo Nature Chemistry, 2013 , vol. 5, # 8 p. 718 - 723]