SEARCH Articles Figures Tables 1,2-Rearrangement of P,y-epoxy alcohols 1- Alkynyl-2,3-epoxy alcohols 1.2- Diols from 0,7-epoxy alcohols 1.2- Epoxy alcohols with thiols 2, 3-Epoxy alcohols, ring openings, with 2,3-epoxy alcohols 2,3-shift 2,3-epoxy alcohols amine nucleophiles, addition 2,3-epoxy alcohols carbon nucleophile addition 2,3-epoxy alcohols carboxylates, opening 2,3-epoxy alcohols ethers 2,3-epoxy alcohols hydride, addition 2,3-epoxy alcohols introduced 2,3-epoxy alcohols nucleophilic epoxide opening 2.3- Epoxy alcohols Subject 2.3- Epoxy alcohols reactions 2.3- Epoxy alcohols with nucleophiles 2.3- epoxy alcohol derivatives A,/?-Epoxy alcohols A,p-Epoxy alcohols Acyclic epoxy alcohols Alcohols 2.3- epoxy primary, oxidation Alcohols epoxy, ring opening Alcohols, 2,3-epoxy regioselective Alcohols, 2,3-epoxy regioselectivity Alcohols, 2,3-epoxy stereochemistry Alcohols, allylic epoxy ketones Alcohols, epoxy metal hydrides Alcohols, epoxy reduction Allylic epoxy alcohols Chiral compounds epoxy alcohols Cyclization of epoxy alcohol Cyclopropanes Epoxy alcohol Diols, 3-azidosynthesis via epoxy alcohols Epoxidation from 2,3-epoxy alcohols Epoxy alcohol fragmentation Epoxy alcohol ring opening intramolecular nucleophile Epoxy alcohol, Payne rearrangement Epoxy alcohols, chiral, ring opening Epoxy alcohols, rearrangement Epoxy-alcohol product Hydroxy ketones from epoxy alcohols P,y-Epoxy alcohols Payne rearrangement, of epoxy alcohol Protected Epoxy Alcohols Regioselectivity epoxy alcohol reduction Silyl epoxy alcohols