The diastereoselective cyclopropanation of three stereoisomerically unique vinylcyclopropanes was studied. The selective preparation of six stereoisomeric bicyclopropanes was accomplished by an iterative reagent-controlled process. With the exception of the cis-syntrans-bicyclopropane, all isomers can be prepared in a diastereomeric excess of greater than 5:1
Dienes, bearing an electron-withdrawing substituent at C-1, are cyclopropanated regio- and stereo se...
A new method is described for the synthesis of diastereomerically pure cyclopropanes from substitute...
A highly diastereoselective cyclopropanation of cyclic enones with sulfur ylides was developed under...
The diastereoselective cyclopropanation of three stereoisomerically unique vinylcyclopropanes was st...
Diastereoselective cyclopropanation of a trans-substituted vinyl cyclopropane was studied. The stere...
Diastereoselective cyclopropanation of a trans-substituted vinyl cyclopropane was studied. The stere...
The identification of two natural products, FR-900848 and U-106305, has stimulated interest concerni...
The identification of two natural products, FR-900848 and U-106305, has stimulated interest concerni...
The identification of two natural products, FR-900848 and U-106305, has stimulated interest concerni...
The reaction of aryl- and vinyl-stabilized sulfonium ylides with electron-poor dienes has been inves...
The stereoselective preparation of three stereoisomeric tercyclopropanes and a quinquecyclopropane w...
The stereoselective preparation of three stereoisomeric tercyclopropanes and a quinquecyclopropane w...
A highly diastereoselective cyclopropanation protocol has been employed in the syntheses of trans-SC...
Cyclopropanation of [2-(alkenyl)pentenediyl]Fe(CO)3 complexes (4) proceeds in a diastereoselective f...
Dienes, bearing an electron-withdrawing substituent at C-1, are cyclopropanated regio- and stereo se...
Dienes, bearing an electron-withdrawing substituent at C-1, are cyclopropanated regio- and stereo se...
A new method is described for the synthesis of diastereomerically pure cyclopropanes from substitute...
A highly diastereoselective cyclopropanation of cyclic enones with sulfur ylides was developed under...
The diastereoselective cyclopropanation of three stereoisomerically unique vinylcyclopropanes was st...
Diastereoselective cyclopropanation of a trans-substituted vinyl cyclopropane was studied. The stere...
Diastereoselective cyclopropanation of a trans-substituted vinyl cyclopropane was studied. The stere...
The identification of two natural products, FR-900848 and U-106305, has stimulated interest concerni...
The identification of two natural products, FR-900848 and U-106305, has stimulated interest concerni...
The identification of two natural products, FR-900848 and U-106305, has stimulated interest concerni...
The reaction of aryl- and vinyl-stabilized sulfonium ylides with electron-poor dienes has been inves...
The stereoselective preparation of three stereoisomeric tercyclopropanes and a quinquecyclopropane w...
The stereoselective preparation of three stereoisomeric tercyclopropanes and a quinquecyclopropane w...
A highly diastereoselective cyclopropanation protocol has been employed in the syntheses of trans-SC...
Cyclopropanation of [2-(alkenyl)pentenediyl]Fe(CO)3 complexes (4) proceeds in a diastereoselective f...
Dienes, bearing an electron-withdrawing substituent at C-1, are cyclopropanated regio- and stereo se...
Dienes, bearing an electron-withdrawing substituent at C-1, are cyclopropanated regio- and stereo se...
A new method is described for the synthesis of diastereomerically pure cyclopropanes from substitute...
A highly diastereoselective cyclopropanation of cyclic enones with sulfur ylides was developed under...