Reaction with formic acid of triarylmethanols containing para-fluorine substituents gives, in addition to the expected triarylmethanes, products in which one fluorine has been replaced by a hydroxy-group; in contrast, pentafluorophenyldiphenylmethanol on similar treatment gives the pentafluorophenyldiphenylmethane together 9-(pentafluorophenyl)-fluorene.</p
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
Reaction with formic acid of triarylmethanols containing para-fluorine substituents gives, in additi...
Triarylmethanols containing one or more fluorine substituants in the para-positions are converted by...
Triarylmethanols containing one or more fluorine substituants in the para-positions are converted by...
Isomeric fluorinated α‐bromoenones react with dinucleophilic β‐mercaptoalcohols in CH2Cl2 at room te...
The trifluoromethyl group is a highly important substituent in organic chemistry. Its powerful elect...
The reactions of formic acid with and without addition of sodium formate with diphenylmethanol (4) a...
International audienceWe report here a novel and easy-to-handle reductive dehalogenation of 9-bromof...
International audienceWe report here a novel and easy-to-handle reductive dehalogenation of 9-bromof...
The efficient synthesis of fluorenes from biaryl triazenes is successfully developed. Up to 27 examp...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
Reaction with formic acid of triarylmethanols containing para-fluorine substituents gives, in additi...
Triarylmethanols containing one or more fluorine substituants in the para-positions are converted by...
Triarylmethanols containing one or more fluorine substituants in the para-positions are converted by...
Isomeric fluorinated α‐bromoenones react with dinucleophilic β‐mercaptoalcohols in CH2Cl2 at room te...
The trifluoromethyl group is a highly important substituent in organic chemistry. Its powerful elect...
The reactions of formic acid with and without addition of sodium formate with diphenylmethanol (4) a...
International audienceWe report here a novel and easy-to-handle reductive dehalogenation of 9-bromof...
International audienceWe report here a novel and easy-to-handle reductive dehalogenation of 9-bromof...
The efficient synthesis of fluorenes from biaryl triazenes is successfully developed. Up to 27 examp...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...
The reactivity of title compound (II) towards simple electron rich and electron poor aromatics is i...