A study on the formation of N-tosyl-1,3,2-oxazaborolidin-5-one by electrospray mass spectrometry
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[1] R. Kostiainen,et al. Mass spectrometric studies on the formation of chiral N-sulphonylated oxazaborolidinones , 1999 .
[2] A. Bruins. Mechanistic aspects of electrospray ionization , 1998 .
[3] S. Kiyooka,et al. Catalyst control in a chiral borane-mediated aldol reaction. Both syn- and anti-aldols in almost optically pure state obtained from one racemic aldehyde , 1996 .
[4] H. W. Scheeren,et al. Asymmetric 13-dipolar cycloaddition of nitrones with ketene acetals catalyzed by chiral oxazaborolidines , 1994 .
[5] H. W. Scheeren,et al. Asymmetric Diels-Alder reactions catalyzed by chiral oxazaborolidines. Effect of the position of an electron-donor functionality in the α-side chain substituent on the enantioselectivity , 1993 .
[6] M. Rose,et al. Negative-ion electrospray and fast atom bombardment mass spectrometry of esters of boron acids , 1992 .
[7] E. Parmee,et al. The catalytic asymmetric aldol reaction of aldehydes with unsubstituted and monosubstituted silyl ketene acetals: formation of anti-β-hydroxy-α-methyl esters , 1992 .
[8] E. Corey,et al. First application of attractive intramolecular interactions to the design of chiral catalysts for highly enantioselective Diels-Alder reactions , 1991 .
[9] E. Corey,et al. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications , 1987 .
[10] L. Dias. Chiral Lewis acid catalysts in diels-Alder cycloadditions: mechanistic aspects and synthetic applications of recent systems , 1997 .