(PDF) Stereocontrolled Route to Vicinal Diamines by Allyl

Stereocontrolled Route to Vicinal Diamines by Allyl Cyanate-Isocyanate Rearrangement: Asymmetric Synthesis of Anti-(2r, 3r)- And Syn-(2r, 3s)-2, 3-Diaminobutanoic Acids

doi 10.1021/ol0621102.s001

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Amanote Research

Stereocontrolled Route to Vicinal Diamines by Allyl Cyanate-Isocyanate Rearrangement: Asymmetric Synthesis of Anti-(2r, 3r)- And Syn-(2r, 3s)-2, 3-Diaminobutanoic Acids

doi 10.1021/ol0621102.s001

Full Text

Abstract

Date

Authors

Publisher

Related search

(2r,3r)-1,4-Dioxaspiro[4.4]nonane-2,3-Dicarboxylic and (2r,3r)-1,4-Dioxaspiro[4.5]decane-2,3-Dicarboxylic Acids

Asymmetric Syntheses via Heterocyclic Intermediates, XLV. Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure 3-Substituted (2r,3s)-Serine Methyl Esters

Asymmetric Reduction of Aromatic Ketones. II. An Enantioselective Synthesis of Methyl(2R,3S)-3-(4-Methoxypehnyl)glycidate.

Crystal Structures of (2s,3s)- And (2r,3s)-N-Tert-Butoxycarbonyl-3-Amino-1-Chloro-2-Hydroxy-4-Phenylbutane

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Synthesis of (2r,3s)-((1r,2s,5r)-2-Isopropyl-5-Methylcyclohexyl) 2-(4-Bromophenyl)-3-(Tert-Butoxy-Carbonylamino)-Tetrahydrofuran-3-Carboxylate and (2s,3r)-((1r,2s,5r)-2-Isopropyl- 5-Methylcyclohexyl)2-(4- Bromophenyl)-3-(Tert-Butoxy¬carbonyl¬amino)-Tetrahydrofuran-3-Carboxylate

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Stereoselective Synthesis of Protected (2R, 3R, 4s)-4, 7-Diamino-2, 3-Dihydroxyheptanoic Acid: A Novel Amino Acid of Callipeltins a and D