Interesting by-products in the synthesis of chiral α-aminophosphinates from enantiopure sulfinimines
摘要:
A new reaction of enantiopure sulfinimines and ethyl phenylphosphinate is given. Several unexpected products were isolated and identified, their mechanism of formation is proposed. (C) 2004 Elsevier Ltd. All rights reserved.
Interesting by-products in the synthesis of chiral α-aminophosphinates from enantiopure sulfinimines
摘要:
A new reaction of enantiopure sulfinimines and ethyl phenylphosphinate is given. Several unexpected products were isolated and identified, their mechanism of formation is proposed. (C) 2004 Elsevier Ltd. All rights reserved.
Diastereoselective Trifluoromethylation of Chiral<i>N</i>-(Tolylsulfinyl)imines in the Presence of Lewis Bases
作者:Yoshikazu Kawano、Teruaki Mukaiyama
DOI:10.1246/cl.2005.894
日期:2005.7
A diastereoselctive trifluoromethylation of chiral N-(tolylsulfinyl)imines with (trifluoromethyl)trimethylsilane in the presence of Lewis bases such as tetrabutylammonium acetate or phenoxide proceeded smoothly to afford the corresponding trifluoromethylated adducts in good yields.
Interesting by-products in the synthesis of chiral α-aminophosphinates from enantiopure sulfinimines
作者:Andrea Szabó、Zsuzsa M Jászay、László Töke、Imre Petneházy
DOI:10.1016/j.tetlet.2003.12.151
日期:2004.2
A new reaction of enantiopure sulfinimines and ethyl phenylphosphinate is given. Several unexpected products were isolated and identified, their mechanism of formation is proposed. (C) 2004 Elsevier Ltd. All rights reserved.