1993
DOI: 10.1080/00397919308009780
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One-Pot Conversion of 1,2-Diols to Epoxides: Convenient Preparation of Methyl 2,3-Anhydro-5-O-trityl-β-D-lyxofuranoside and Methyl 2,3-Anhydro-4,6-O-benzylidene-α-D-mannopyranoside

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Cited by 12 publications
(1 citation statement)
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“…We have reexamined this modification for terminal alkene substrates (see below) but have not been able to achieve improved enantiofacial selectivities [vis - à-vis the use of K 3 Fe(CN) 6 ]. Finally, since 1,2-diols can be easily converted by a variety of methods into 1,2-epoxides, it is also relevant that there are no effective methods for direct asymmetric epoxidation of alkenes such as 1 to give 1,2-epoxy analogues of 2 . ,
1
…”
Section: Introductionmentioning
confidence: 99%
“…We have reexamined this modification for terminal alkene substrates (see below) but have not been able to achieve improved enantiofacial selectivities [vis - à-vis the use of K 3 Fe(CN) 6 ]. Finally, since 1,2-diols can be easily converted by a variety of methods into 1,2-epoxides, it is also relevant that there are no effective methods for direct asymmetric epoxidation of alkenes such as 1 to give 1,2-epoxy analogues of 2 . ,
1
…”
Section: Introductionmentioning
confidence: 99%