Diastereoselective Addition of Amines to Vinyl Sulfone Modified Carbohydrates: A Highly Flexible Methodology for the Synthesis of New Classes of Deoxyaminosugars-Reference-Cited by-同舟云学术

Diastereoselective Addition of Amines to Vinyl Sulfone Modified Carbohydrates: A Highly Flexible Methodology for the Synthesis of New Classes of Deoxyaminosugars

Published:2000-03-30 Issue:9 Volume:65 Page:2637-2641
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ravindran Bindu¹,Sakthivel Kandasamy¹,Suresh Cheravakkattu. G.¹,Pathak Tanmaya¹

Affiliation:

1. Organic Chemistry Division (Synthesis) and bDivision of Biochemical Sciences, National Chemical Laboratory, Pune 411 008, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo991380d

Reference16 articles.

1. A facile synthesis of derivatives of lividosamine, a component of lividomycin B

2. Polyamino sugars IV. A synthesis of a new type of nucleosides: methyl 4,6--benzylidene-2,3-dideoxy-3-nitro-2-(7′-theophyllinyl)-β-D-glucopyranoside and its 2-(2′,6′-dichloro-9′-purinyl) homolog.

3. A new synthesis of 2,3-diamino-2,3-dideoxy-D-glucose

4. 3′-Deoxy-3′-(vinylsulphonyl)thymidine — a new reactive analogue of AZT: its synthesis and reactivities towards various nucleophiles

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