Synthesis of unnatural 2R,5S-5-hydroxypipecolic acid via homochiral acyliminium ion - pipecolic acids - part III.
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference19 articles.
1. Part II: C. Herdeis and W. Engel, Arch. Pharm. (Weinheim) in print.
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3. Proof of delocalization-stabilization by sulfur in enolate formation during racemisation of sulfur containing amino acid residues.
4. Tin tetrachloride-induced π-cyclizations of glycine cation equivalents to substituted pipecolic acid derivatives
5. Chiral synthesis of 5-hydroxy-(L)-pipecolic acids from (L)-glutamic acid
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1. A new facile synthesis of (2S,5S)-5-hydroxypipecolic acid hydrochloride;Synthetic Communications;2022-03-19
2. An expedient synthesis of cyanoformates via DAST-mediated C C bond cleavage of α-oximino-β-ketoesters;Tetrahedron Letters;2021-06
3. Complementary and Stereodivergent Approaches to the Synthesis of 5-Hydroxy- and 4,5-Dihydroxypipecolic Acids from Enantiopure Hydroxylated Lactams;European Journal of Organic Chemistry;2013-01-21
4. Spectroscopic and X-ray Crystallographic Evidence for Electrostatic Effects in 4-Substituted Cyclohexanone-Derived Hydrazones, Imines, and Corresponding Salts;The Journal of Organic Chemistry;2011-09-14
5. ChemInform Abstract: Pipecolic Acids. Part 3. Synthesis of Unnatural 2R,5S-5- Hydroxypipecolic Acid via Homochiral Acyliminium Ion.;ChemInform;2010-08-22
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