A novel mode of reductive elimination from a 2-deoxy-2-iodo-α-d-altropyranoside
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference11 articles.
1. THE PREPARATION OF 4,6-O-BENZYLIDENE-D-GLUCAL AND THE REACTION OF METHYLLITHIUM WITH METHYL 2,3-ANHYDRO-4,6-O-BENZYLIDENE-α-D-ALLOPYRANOSIDE
2. Preparation of unsaturated carbohydrates. A facile synthesis of methyl 4,6-O-Benzylidene-D-hex-2-enopyranosides
3. A facile synthesis of D-allal and its derivatives
4. Some acetals of methyl 2-deoxy-2-halogeno-α-D-altropyranoside and their reactions with lithium aluminium hydride
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3. Tuning the Stereoelectronic Properties of 1-Sulfanylhex-1-enitols for the Sequential Stereoselective Synthesis of 2-Deoxy-2-iodo-β-d-allopyranosides;The Journal of Organic Chemistry;2014-03-21
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5. Organofluorine compounds and fluorinating agents, 10. Unusual regio- and stereoselective 3,4-acetalizations of selected pyranosides by hexafluoroacetone as a result of a new reaction pathway;Liebigs Annalen der Chemie;1994-02-14
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