(PDF) Synthesis of 2s,5s-And 2r,5s-5-Hydroxypipecolic Acid

Synthesis of 2s,5s-And 2r,5s-5-Hydroxypipecolic Acid via Amide-Methylenation of S-5-Hydroxy-2-Piperidone With Dimethyltitanocene.

Tetrahedron Asymmetry - United Kingdom

doi 10.1016/s0957-4166(00)82257-0

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Abstract

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Date

January 1, 1993

Authors

Claus Herdeis

Eberhard Heller

Publisher

Elsevier BV

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Amanote Research

Synthesis of 2s,5s-And 2r,5s-5-Hydroxypipecolic Acid via Amide-Methylenation of S-5-Hydroxy-2-Piperidone With Dimethyltitanocene.

Tetrahedron Asymmetry - United Kingdom

doi 10.1016/s0957-4166(00)82257-0

Full Text

Abstract

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Date

Authors

Publisher

Related search

Synthesis and Molecular Structure of Chiral (2S, 5s)-Tert-Butyl 3-Oxo-2-Oxa-5-Azabicyclo[2.2.2]octane-5-Carboxylate

(5s)-3-Chloro-4-Diallylamino-5-[(1r,2s,5r)-2-Isopropyl-5-Methylcyclohexyloxy]furan-2(5h)-One

(2s,3s)-1-Phenylthio-2,3-Butanediol. A Useful Chiral Building Block for a Simple Syntheses of (4r,5s)-5-Hydroxyhexan-4-Olide and (4r,5s)-5-Hydroxy-2-Hexen-4-Olide

Synthesis of Chiral Pyrrolidine Derivatives From (S)-Pyroglutamic Acid. I: 7-Substituted (2r,5s)-2-Aryl-1-Aza-3-Oxabicyclo(3.3.0)octan-8-Ones, 7-Substituted (2r,5s)-2-Aryl-1-Aza-3-Oxabicyclo(3.3.0)oct-6-En-8-Ones and 3-Substituted (S)-5-(Hydroxymethyl)-2-Pyrrolidinones.

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