1255574-23-2Relevant academic research and scientific papers
CuCl/bipyridine-catalyzed addition reactions of arylboroxines with aldehydes, α,β-unsaturated ketones, and N-tosyl aldimines
Liao, Yuan-Xi,Hu, Qiao-Sheng
experimental part, p. 7602 - 7607 (2011/11/12)
CuCl/bipyridine-catalyzed addition reactions of arylboroxines with aldehydes and α,β-unsaturated ketones at elevated temperatures were described. By using the microwave energy, CuCl/bipyridine-catalyzed addition reactions of arylboroxines with aldimines were also realized.
Enders SAMP-hydrazone as traceless auxiliary in the asymmetric 1,4-addition of cuprates to enones
Sammet, Karsten,Gastl, Christoph,Baro, Angelika,Laschat, Sabine,Fischer, Peter,Fettig, Ina
supporting information; experimental part, p. 2281 - 2290 (2010/12/29)
Conjugate additions of Gilman cyanocuprates to (5)-N-amino-2- (methoxymethyl)pyrrolidine (SAMP)-hydrazones 4, 5 derived from cyclic and acyclic α,β-unsaturated ketones were investigated. A protocol utilizing copper(II) sulfate/ammonium chloride was evolved, which allowed cleavage of SAMP (S)-1 under the hydrolysis and work-up conditions, followed by recovery of the auxiliary with ethylenediaminetetraacetic acid (EDTA). The enantioselectivity of cuprate additions was dominated for cyclic SAMP-hydrazones 4 by the cuprate alkyl substituent and the ring size, in the case of acyclic arylidene SAMP-hydrazones 5, however, by the nature of the aryl substituent. Electron-donating substituents gave poor enantiomeric excesses, whereas electron-withdrawing groups provided excellent ee values of 98-99%. The configuration of the new stereocenter was determined to be (R). Moreover, a reaction sequence was developed which integrates a tandem 1,4-addition/ methylation and traceless hydrolytic cleavage of the auxiliary (S)-1 in a one-pot reaction, resulting in enantiomerically pure methyl ketones 11-13, each of them with > 99% ee.
