piperidines and 3-hydroxypipecolic-acid

piperidines has been researched along with 3-hydroxypipecolic-acid* in 3 studies

Other Studies

3 other study(ies) available for piperidines and 3-hydroxypipecolic-acid

ArticleYear
Synthesis of (+)-L-733,060, (+)-CP-99,994 and (2S,3R)-3-hydroxypipecolic acid: application of an organocatalytic direct vinylogous aldol reaction.
    Organic & biomolecular chemistry, 2012, Mar-14, Volume: 10, Issue:10

    The γ-butenolide obtained from an organocatalyzed, direct vinylogous aldol reaction of γ-crotonolactone and benzaldehyde serves as the key starting material in the expedient synthesis of a 3-hydroxy-2-phenyl piperidine intermediate which is converted to the target 2,3-disubstituted piperidines.

    Topics: Aldehydes; Catalysis; Pipecolic Acids; Piperidines

2012
Synthesis of (-)-deoxoprosophylline, (+)-2-epi-deoxoprosopinine, and (2R,3R)- and (2R,3S)-3-hydroxypipecolic acids from D-glycals.
    The Journal of organic chemistry, 2010, Jul-02, Volume: 75, Issue:13

    New syntheses of (-)-deoxoprosophylline, (+)-2-epi-deoxoprosopinine, and (2R,3R)- and (2R,3S)-3-hydroxypipecolic acids are reported. Utilization of the chiral functionalities of Perlin aldehydes, derived from 3,4,6-tri-O-benzyl glycals, has been done along with chemoselective saturation of olefins and reductive aminations as key steps.

    Topics: Alkaloids; Benzyl Compounds; Molecular Structure; Pipecolic Acids; Piperidines; Pyrans; Stereoisomerism

2010
Chiron approach to the synthesis of (2S,3R)-3-hydroxypipecolic acid and (2R,3R)-3-hydroxy-2-hydroxymethylpiperidine from D-glucose.
    The Journal of organic chemistry, 2008, May-02, Volume: 73, Issue:9

    The first chiron approach from d-glucose for the total synthesis of (2 S,3 R)-3-hydroxypipecolic acid (-)-1a and (2R,3R)-3-hydroxy-2-hydroxymethylpiperidine (-)-2a is reported. The synthetic pathway involves conversion of d-glucose into 3-azidopentodialdose (5) followed by the Wittig olefination and reduction to give the piperidine ring skeleton (8) with a sugar appendage that on cleavage of an anomeric carbon followed by oxidation gives (-)-1a which on reduction affords (-)-2a.

    Topics: Catalysis; Glucose; Hydrogen; Metals; Molecular Structure; Pipecolic Acids; Piperidines; Viral Vaccines

2008