(Q57697160)

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A highly stereoselective entry to α-hydroxy carboxylic acids using d-fructose diacetonide as a chiral auxiliary

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A highly stereoselective entry to α-hydroxy carboxylic acids using d-fructose diacetonide as a chiral auxiliary (English)

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1 reference

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Hongwu Yu

1

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C.Eric Ballard

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2

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Binghe Wang

series ordinal

3

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publication date

March 2001

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published in

Tetrahedron Letters

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volume

42

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issue

10

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page(s)

1835-1838

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cites work

Tamandarins A and B: new cytotoxic depsipeptides from a Brazilian ascidian of the family Didemnidae

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7 January 2021

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Synthesis of cryptophycin 52 using the sharpless asymmetric dihydroxylation: diol to epoxide transformation optimized for a base-sensitive substrate

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7 January 2021

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Yanucamides A and B, two new depsipeptides from an assemblage of the marine cyanobacteria Lyngbya majuscula and Schizothrix species

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Kulolide: A Cytotoxic Depsipeptide from a Cephalaspidean Mollusk,Philinopsis speciosa1

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Malevamides A−C, New Depsipeptides from the Marine CyanobacteriumSymploca laete-viridis

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Asymmetric hydroxylation of enolates with N-sulfonyloxaziridines

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7 January 2021

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Asymmetric oxygenation of chiral imide enolates. A general approach to the synthesis of enantiomerically pure .alpha.-hydroxy carboxylic acid synthons

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7 January 2021

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Dynamic kinetic resolution of alpha-hydroxy acid esters

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7 January 2021

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Diastereoselective alkylations of oxazolidinone glycolates: a useful extension of the Evans asymmetric alkylation

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An Efficient Catalytic Asymmetric Epoxidation Method

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7 January 2021

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Highly diastereoselective Diels-Alder reactions using a fructose diacetonide chiral scaffold

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Synthesis of analogs of 1,3-dihydroxyacetone phosphate and glyceraldehyde 3-phosphate for use in studies of fructose-1,6-diphosphate aldolase

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10.1016/S0040-4039(01)00043-0

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(Q57697160)

A highly stereoselective entry to α-hydroxy carboxylic acids using d-fructose diacetonide as a chiral auxiliary

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