A one-pot synthesis of epoxides from commercially available benzyl alcohols and aldehydes is described. The reaction proceeds through in situ generation of sulfonium salts from benzyl alcohols and their subsequent deprotonation for use in Corey–Chaykovsky epoxidation of aldehydes. The generality of the method is exemplified by the synthesis of 34 epoxides that were made from an array of electronically and sterically varied alcohols and aldehydes
Facile one-pot synthesis of syn-2,3-epoxyalcohols from a,P-unsaturated ketones was achieved by conse...
ABSTRACT: The first catalytic, highly C3-selective, stereosepecific ring-opening reaction of 2,3-epo...
Facile one-pot synthesis of syn-2,3-epoxyalcohols from α,β-unsaturated ketones was achieved by conse...
The transformation of epoxides into other compounds by exploiting the reactivity of the oxirane ring...
Treatment of (1RS, SSR)-(1-phenylsulfinyl-2-valeryl benzene) chromium tricarbonyl 2 with a sulfur yl...
Treatment of (1RS, SSR)-(1-phenylsulfinyl-2-valeryl benzene) chromium tricarbonyl 2 with a sulfur yl...
The transformation of epoxides into other compounds by exploiting the reactivity of the oxirane ring...
In recent years, there has been an increased effort to introduce green chemistry principles into org...
In order to produce a highly functionalized five-membered ring useful for further synthetic processe...
In recent years, there has been an increased effort to introduce green chemistry principles into org...
In recent years, there has been an increased effort to introduce green chemistry principles into org...
In recent years, there has been an increased effort to introduce green chemistry principles into org...
Abstract Oxidative functionalization of alkenes is a versatile strategy for the preparation of many ...
A simple, efficient, stereoselective, and regioselective method for the synthesis of beta-alkoxy alc...
Facile one-pot synthesis of syn-2,3-epoxyalcohols from a,P-unsaturated ketones was achieved by conse...
Facile one-pot synthesis of syn-2,3-epoxyalcohols from a,P-unsaturated ketones was achieved by conse...
ABSTRACT: The first catalytic, highly C3-selective, stereosepecific ring-opening reaction of 2,3-epo...
Facile one-pot synthesis of syn-2,3-epoxyalcohols from α,β-unsaturated ketones was achieved by conse...
The transformation of epoxides into other compounds by exploiting the reactivity of the oxirane ring...
Treatment of (1RS, SSR)-(1-phenylsulfinyl-2-valeryl benzene) chromium tricarbonyl 2 with a sulfur yl...
Treatment of (1RS, SSR)-(1-phenylsulfinyl-2-valeryl benzene) chromium tricarbonyl 2 with a sulfur yl...
The transformation of epoxides into other compounds by exploiting the reactivity of the oxirane ring...
In recent years, there has been an increased effort to introduce green chemistry principles into org...
In order to produce a highly functionalized five-membered ring useful for further synthetic processe...
In recent years, there has been an increased effort to introduce green chemistry principles into org...
In recent years, there has been an increased effort to introduce green chemistry principles into org...
In recent years, there has been an increased effort to introduce green chemistry principles into org...
Abstract Oxidative functionalization of alkenes is a versatile strategy for the preparation of many ...
A simple, efficient, stereoselective, and regioselective method for the synthesis of beta-alkoxy alc...
Facile one-pot synthesis of syn-2,3-epoxyalcohols from a,P-unsaturated ketones was achieved by conse...
Facile one-pot synthesis of syn-2,3-epoxyalcohols from a,P-unsaturated ketones was achieved by conse...
ABSTRACT: The first catalytic, highly C3-selective, stereosepecific ring-opening reaction of 2,3-epo...
Facile one-pot synthesis of syn-2,3-epoxyalcohols from α,β-unsaturated ketones was achieved by conse...