1034147-67-5Relevant academic research and scientific papers
A facile formal [2+1] cycloaddition of styrenes with alpha-bromocarbonyls catalyzed by copper: Efficient synthesis of donor-acceptor cyclopropanes
Nishikata, Takashi,Noda, Yushi,Fujimoto, Ryo,Ishikawa, Shingo
supporting information, p. 12843 - 12846 (2015/08/18)
Reactions of 2-bromoesters and styrenes underwent a [2+1] cycloaddition reaction, i.e., cyclopropanation, to produce donor-acceptor (D-A) cyclopropanes through a radical addition-ring closure process. In this reaction, the combination of copper(ii) comple
Scope and mechanism for Lewis acid-catalyzed cycloadditions of aldehydes and donor-acceptor cyclopropanes: Evidence for a stereospecific intimate ion pair pathway
Pohlhaus, Patrick D.,Sanders, Shanina D.,Parsons, Andrew T.,Li, Wei,Johnson, Jeffrey S.
, p. 8642 - 8650 (2008/12/23)
In this work, the one-step diastereoselective synthesis of cis-2,5-disubstituted tetrahydrofurans via Lewis acid catalyzed [3 + 2] cycloadditions of donor-acceptor (D-A) cyclopropanes and aldehydes is described. The scope and limitations with respect to both reaction partners are provided. A detailed examination of the mechanism has been performed, including stereochemical analysis and electronic profiling of both reactants. Experimental evidence supports an unusual stereospecific intimate ion pair mechanism wherein the aldehyde functions as a nucleophile and malonate acts as the nucleofuge. The reaction proceeds with inversion at the cyclopropane donor site and allows absolute stereochemical information to be transferred to the products with high fidelity. The mechanism facilitates the stereospecific synthesis of a range of optically active tetrahydrofuran derivatives from enantioenriched D-A cyclopropanes.
