ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE

The potential of D-glucuronolactone as a starting material for the synthesis of polyfunctional amino acids is illustrated by its conversion to 2S,3R,4R,5S-trihydroxypipecolic acid, 2R,3R,4R,5S-trihydroxypipecolic acid, 2S,4S,5S-dihydroxypipecolic acid, and bulgecinine. © 1986.

Bibliografiset tiedot
Päätekijät: Bashyal, B, Chow, H, Fleet, G
Aineistotyyppi: Journal article
Kieli:English
Julkaistu: 1986
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author Bashyal, B
Chow, H
Fleet, G
author_facet Bashyal, B
Chow, H
Fleet, G
author_sort Bashyal, B
collection OXFORD
description The potential of D-glucuronolactone as a starting material for the synthesis of polyfunctional amino acids is illustrated by its conversion to 2S,3R,4R,5S-trihydroxypipecolic acid, 2R,3R,4R,5S-trihydroxypipecolic acid, 2S,4S,5S-dihydroxypipecolic acid, and bulgecinine. © 1986.
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spelling oxford-uuid:cec8384a-44d7-40ef-a3ed-a8d9cd47bed82022-03-27T07:38:03ZENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONEJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:cec8384a-44d7-40ef-a3ed-a8d9cd47bed8EnglishSymplectic Elements at Oxford1986Bashyal, BChow, HFleet, GThe potential of D-glucuronolactone as a starting material for the synthesis of polyfunctional amino acids is illustrated by its conversion to 2S,3R,4R,5S-trihydroxypipecolic acid, 2R,3R,4R,5S-trihydroxypipecolic acid, 2S,4S,5S-dihydroxypipecolic acid, and bulgecinine. © 1986.
spellingShingle Bashyal, B
Chow, H
Fleet, G
ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE
title ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE
title_full ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE
title_fullStr ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE
title_full_unstemmed ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE
title_short ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE
title_sort enantiospecific syntheses of 2s 3r 4r 5s trihydroxypipecolic acid 2r 3r 4r 5s trihydroxypipecolic acid 2s 4s 5s dihydroxypipecolic acid and bulgecinine from deuterium glucuronolactone
work_keys_str_mv AT bashyalb enantiospecificsynthesesof2s3r4r5strihydroxypipecolicacid2r3r4r5strihydroxypipecolicacid2s4s5sdihydroxypipecolicacidandbulgecininefromdeuteriumglucuronolactone
AT chowh enantiospecificsynthesesof2s3r4r5strihydroxypipecolicacid2r3r4r5strihydroxypipecolicacid2s4s5sdihydroxypipecolicacidandbulgecininefromdeuteriumglucuronolactone
AT fleetg enantiospecificsynthesesof2s3r4r5strihydroxypipecolicacid2r3r4r5strihydroxypipecolicacid2s4s5sdihydroxypipecolicacidandbulgecininefromdeuteriumglucuronolactone