Polyhydroxylated pyrrolidines, III. Synthesis of new protected 2,5-dideoxy-2,5-iminohexitols from d-fructose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. A practical route to partially protected pyrrolidines as precursors for the stereoselective synthesis of alexines
2. Polyhydroxylated pyrrolidines. Part II: Highly stereoselective synthesis of partially protected DMDP derivatives from d-fructose
3. Polyhydroxylated pyrrolizidines. Part 2: The first total synthesis of (+)-hyacinthacine A3
4. Polyhydroxylated pyrrolizidines. Part 3: A new and short enantiospecific synthesis of (+)-hyacinthacine A2
5. Polyhydroxylated pyrrolizidines. Part 6: A new and concise stereoselective synthesis of (+)-casuarine and its 6,7-diepi isomer, from DMDP
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1. Synthesis of α-Acyloxynitrones and Reactivity towards Samarium Diiodide;European Journal of Organic Chemistry;2016-07-26
2. Synthesis of γ-Azido-β-ureido Ketones and Their Transformation into Functionalized Pyrrolines and Pyrroles via Staudinger/aza-Wittig Reaction;The Journal of Organic Chemistry;2013-01-10
3. Glycosidase Inhibition by All 10 Stereoisomeric 2,5-Dideoxy-2,5-iminohexitols Prepared from the Enantiomers of Glucuronolactone;The Journal of Organic Chemistry;2012-09-06
4. Synthesis of the Proposed Structure of Pentahydroxylated Pyrrolizidine Hyacinthacine C5 and Its C6,C7 Epimer;European Journal of Organic Chemistry;2011-10-17
5. Synthesis of unnatural pentahydroxylated pyrrolizidines: 5-epi- and 5,7a-di-epi-hyacinthacine C1;Tetrahedron;2010-09
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