Preparation of 2-amino-1,6-anhydro-2,3-dideoxy-β-d-arabino-hexopyranose. 1H- and 13C-n.m.r. spectra of deoxy derivatives of 2-amino-1,6-anhydro-2-deoxy-d-glucose and 2-amino-1,6-anhydro-2-deoxy-d-mannose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference20 articles.
1. Preparation of 2-amino-2,4-dideoxy-D-lyxo-hexopyranose (4-deoxy-D-mannosamine) from 1,6-anhydro-β-D-glucopyranose
2. Azido derivatives of 1,6-anhydro-β-D-hexopyranoses corresponding to 3-deoxy- and 4-deoxy-D-glucosamine
3. Preparation of 1,6-anhydro-2,3-dideoxy-2,3-epimino-β-D-mannopyranose and its conversion to 2-amino-1,6-anhydro-2-deoxy-β-D-mannopyranose
4. Preparation of 4-amino-1,6-anhydro-4-deoxy-β-D-glucopyranose. Isomerization of 4-amino-1,6 : 2,3-dianhydro-4-deoxy-β-D-mannopyranose to 1,6-anhydro-3,4-dideoxy-3,4-epimino-β-D-altropyranose
5. Preparation of 2-amino-1,6-anhydro-2-deoxy-β-D-mannopyranose by intramolecular substitution of the tosyloxy group in sterically hindered position of 1,6-anhydro-2-O-p-tolylsulfonyl-β-D-glucopyranose
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