Carbohydrate Homologation by the Use of 2-(Trimethylsilyl)thiazole. Preparative Scale Synthesis of Rare Sugars: l-Gulose, l-Idose, and the Disaccharide Subunit of Bleomycin A2-Reference-Cited by-同舟云学术

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Carbohydrate Homologation by the Use of 2-(Trimethylsilyl)thiazole. Preparative Scale Synthesis of Rare Sugars: l-Gulose, l-Idose, and the Disaccharide Subunit of Bleomycin A2

Published:1997-09-01 Issue:18 Volume:62 Page:6261-6267
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dondoni Alessandro¹,Marra Alberto¹,Massi Alessandro¹

Affiliation:

1. Dipartimento di Chimica, Laboratorio di Chimica Organica, Università, 44100 Ferrara, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo970601h

Reference42 articles.

1. Natural and artificial bleomycins: chemistry and antitumour activities

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1. Synthesis of l-Rare Sugars from d-Sorbitol Using a TiO₂ Photocatalyst;ACS Sustainable Chemistry & Engineering;2023-06-08

2. Synthesis of Four Orthogonally Protected Rare l-Hexose Thioglycosides from d-Mannose by C-5 and C-4 Epimerization;Molecules;2022-05-25

3. A gulose moiety contributes to the belomycin (BLM) disaccharide selective targeting to lung cancer cells;European Journal of Medicinal Chemistry;2021-12

4. Efficient whole-cell biosynthesis of l-gulose by coupling mannitol-1-dehydrogenase with NADH oxidase;Enzyme and Microbial Technology;2021-08

5. Organosilicon azoles: Structure, silylotropy and NMR spectroscopy;Advances in Heterocyclic Chemistry;2021

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