Highly Influential Citations1
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The syn-selective addition of organozinc compounds to 4α-epoxypyranosides (4α-EPs), generated from methyl β-d-glucoside or aminoglucoside, provides an efficient route to pyranosides with α-l-ido… Continue Reading
Reactions of aziridines and epoxides with acetic anhydride catalyzed by an organophosphine provided the corresponding esters of β-amino alcohols and 1,2-diols in high yields, respectively.
Tributylphosphine was found to be an effective promoting reagent for the ring-opening reaction of various epoxides and aziridines with nucleophile to produce corresponding anti-bifunctional products… Continue Reading
[reaction: see text] An orthogonal sulfation strategy involving six different protecting groups has been developed for generating sulfated carbohydrate libraries based on heparan. Chemoselective… Continue Reading
A general approach to formation of the P-ylide from the reaction of aziridines or epoxides with organophosphine under neutral and metal-free conditions is realized. Conjugated diene derivatives based… Continue Reading
Potassium fluoride combined with tetrabutylammonium bisulfate is an efficient reagent to convert a variety of aziridines derived from cyclic and acyclic alkenes to beta-fluoro amine derivatives in… Continue Reading
Tributylphosphine was found to be an effective promoting reagent for ring opening of a variety of aziridines and nucleophiles to produce anti-bifunctional products in good to excellent yield. The… Continue Reading