Asymmetric Synthesis of Both the Enantiomers of trans-3-Hydroxypipecolic Acid
Authors:
- 26 November 2004
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 70 (1) , 360-363
Abstract
Both the enantiomers of trans-3-hydroxypipecolic acid have been synthesized employing the Sharpless asymmetric dihydroxylation and epoxidation as the key steps starting from a commercially available starting material 1,4-butanediol.Keywords
This publication has 37 references indexed in Scilit:
- Saturated nitrogen heterocyclesJournal of the Chemical Society, Perkin Transactions 1, 1999
- 1-Aza Sugars, Apparent Transition State Analogues of Equatorial Glycoside Formation/CleavageAccounts of Chemical Research, 1998
- Saturated nitrogen heterocyclesContemporary Organic Synthesis, 1997
- Chemical and Electrochemical Asymmetric Dihydroxylation of Olefins in I2−K2CO3−K2OsO2(OH)4 and I2−K3PO4/K2HPO4−K2OsO2(OH)4 Systems with Sharpless' LigandThe Journal of Organic Chemistry, 1996
- Catalytic Asymmetric DihydroxylationChemical Reviews, 1994
- Pyrrole, pyrrolidine, piperidine, pyridine, and azepine alkaloidsNatural Product Reports, 1992
- Chirospecific synthesis of .beta.-hydroxy .alpha.-amino acidsThe Journal of Organic Chemistry, 1989
- Pyrrole, pyrrolidine, piperidine, pyridine, and azepine alkaloidsNatural Product Reports, 1989
- Asymmetric Epoxidation of Allylic Alcohols: The Sharpless EpoxidationSynthesis, 1986
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980