The use of aldonolactones for the synthesis of 2-O-methyl-l-rhamnose and 2-O-methyl-d-mannose-Reference-Cited by-同舟云学术

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The use of aldonolactones for the synthesis of 2-O-methyl-l-rhamnose and 2-O-methyl-d-mannose

Published:1989-08 Issue:1 Volume:191 Page:130-137
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Jeroncic Lucio O.,Sznaidman Marcos L.,Cirelli Alicia Fernandez,de Lederkremer Rosa M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference31 articles.

1. Partial Benzoylation of L-Rhamnono and D-Mannono-1,4-Lactone

2. Synthesis of Aldofuranosyl Nucleosides1

3. β-Elimination in aldonolactones. Synthesis of 3,6-dideoxy L-arabino-hexose (ascarylose)

4. Methylation of carbohydrates bearing base-labile substituents, with diazomethane-boron triflouride etherate. I

5. Alkylation of Carbohydrates with Alkyl Trifluoromethanesulfonates.

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Preparation of C-3,5-Acyl Furanoses via Highly Selective Intramolecular Acyl Migration;The Journal of Organic Chemistry;2004-10-01

2. M;Dictionary of Carbohydrates;1998

3. Synthetic Reactions of Aldonolactones;Advances in Carbohydrate Chemistry and Biochemistry;1994

4. Regioselective Acylations of Aldono-1,4-lactones;Journal of Carbohydrate Chemistry;1993-10

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