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HIGHLY REGIOSELECTIVE ALKYLATION AT THE MORE HINDERED ALPHA-SITE OF UNSYMMETRICAL KETONES BY USE OF THEIR POTASSIUM ENOLATES - A COMPARATIVE-STUDY WITH LITHIUM ENOLATES
Authors: QUESNEL Y BIDOISSERY L POIRIER JM DUHAMEL L
Citation: Y. Quesnel et al., HIGHLY REGIOSELECTIVE ALKYLATION AT THE MORE HINDERED ALPHA-SITE OF UNSYMMETRICAL KETONES BY USE OF THEIR POTASSIUM ENOLATES - A COMPARATIVE-STUDY WITH LITHIUM ENOLATES, Synlett, (4), 1998, pp. 413
A CONVENIENT SYNTHESIS OF 2-CHLOROPHENYL METHYLIDENE-5,5-DIMETHYLCYCLOPENTANONE, A KEY INTERMEDIATE FOR A POTENT FUNGICIDE AGAINST BOTRYTIS-CINERA
Authors: QUESNEL Y BIDOISSERY L POIRIER JM DUHAMEL L
Citation: Y. Quesnel et al., A CONVENIENT SYNTHESIS OF 2-CHLOROPHENYL METHYLIDENE-5,5-DIMETHYLCYCLOPENTANONE, A KEY INTERMEDIATE FOR A POTENT FUNGICIDE AGAINST BOTRYTIS-CINERA, Journal of organic chemistry, 63(11), 1998, pp. 3793-3794
HIGHLY SELECTIVE RING-OPENING OF 1,3,3-TRIHALOGENOEPOXYCYCLOHEXANES BY BORON TRIHALIDES - METHODOLOGY FOR THE DETERMINATION OF THE REGIOSELECTIVITY IN THE CYCLIZATION OF 2,2,6,6-TETRAHALOGENOCYCLOHEXANOLS
Authors: DUHAMEL P LEBLOND B BIDOISSERY L POIRIER JM
Citation: P. Duhamel et al., HIGHLY SELECTIVE RING-OPENING OF 1,3,3-TRIHALOGENOEPOXYCYCLOHEXANES BY BORON TRIHALIDES - METHODOLOGY FOR THE DETERMINATION OF THE REGIOSELECTIVITY IN THE CYCLIZATION OF 2,2,6,6-TETRAHALOGENOCYCLOHEXANOLS, Journal of the Chemical Society. Perkin transactions. I, (16), 1994, pp. 2265-2271
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