52745-75-2Relevant articles and documents
Total synthesis and stereochemical assignment of the quinquecyclopropane-containing cholesteryl ester transfer protein inhibitor U-106305
Barrett, Anthony G. M.,Hamprecht, Dieter,White, Andrew J. P.,Williams, David J.
, p. 7863 - 7864 (1996)
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Highly stereoselective cyclopropanation of α,β-unsaturated carbonyl compounds with methyl (diazoacetoxy)acetate catalyzed by a chiral ruthenium(II) complex
Chanthamath, Soda,Takaki, Suguru,Shibatomi, Kazutaka,Iwasa, Seiji
supporting information, p. 5818 - 5821 (2013/07/11)
Tantalizing triangles: The title reaction gives bicarbonyl cyclopropane products that can lead to versatile intermediates with high yields and stereoselectivities. This system was also applied to the enantioselective total synthesis of spiro cyclopropane oxindole, an HIV-1 nonnucleoside reverse transcriptase inhibitor. Copyright
Synthetic methodology for the construction of structurally diverse cyclopropanes
Taylor,Engelhardt,Schmitt,Yuan
, p. 2964 - 2969 (2007/10/03)
Practical and efficient routes for the stereoselective conversion of homoallylic alchols to diastereomerically pure cis-, trans-1,2-disubstituted, and 1,2,3-trisubstituted cyclopropanes have been developed. The routes are highlighted by olefin metathesis