6931-71-1Relevant articles and documents
Sml2-promoted reformatsky-type reaction and acylation of alkyl 1-chlorocyclopropanecarboxylates
Nagano, Takao,Motoyoshiya, Jiro,Kakehi, Akikazu,Nishii, Yoshinori
supporting information; experimental part, p. 5453 - 5456 (2009/06/28)
(Chemical Equation Presented) In the presence of HMPA in THF, highly stereoselective Sml2-promoted substitutions of alkyl 1-chlorocyclopropanecarboxylates 1 using various ketones, aldehydes (Reformatsky-type reaction), and acyl chlorides (acyla
New insights into the mechanism of the McMurry reaction
Villiers, Claude,Ephritikhine, Michel
, p. 2380 - 2382 (2007/10/03)
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TiCl4/Mg/BrCH2CH2Br Reagent System: A 1,2-Diorganometallic Equivalent
Rao, S. Achyutha,Periasamy, M.
, p. 1583 - 1586 (2007/10/02)
1,2-Diorganometallic species generated utilizing the TiCl4/Mg/BrCH2CH2/Br reagent system reacts with ketones to give the corresponding 1,4-diols and/or 1,2-diols in moderate yields.