Diastereoselective Synthesis of Salacinol-Type α-Glucosidase Inhibitors-Reference-Cited by-同舟云学术

Diastereoselective Synthesis of Salacinol-Type α-Glucosidase Inhibitors

Published:2017-12-14 Issue:1 Volume:83 Page:185-193
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ishikawa Fumihiro^ORCID,Jinno Kazumi,Kinouchi Eri,Ninomiya Kiyofumi,Marumoto Shinsuke,Xie Weijia¹,Muraoka Osamu,Morikawa Toshio^ORCID,Tanabe Genzoh^ORCID

Affiliation:

1. State Key Laboratory of Natural Medicines and Department of Medicinal Chemistry, China Pharmaceutical University, Nanjing 210009, P. R. China

Funder

Houansha Foundation

Ministry of Education, Culture, Sports, Science and Technology

Japan Society for the Promotion of Science

Kobayashi International Scholarship Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b02566

Reference31 articles.

1. Salacinol, potent antidiabetic principle with unique thiosugar sulfonium sulfate structure from the Ayurvedic traditional medicine Salacia reticulata in Sri Lanka and India

2. Absolute Stereostructure of Potent α-Glucosidase Inhibitor, Salacinol, with Unique Thiosugar Sulfonium Sulfate Inner Salt Structure from Salacia reticulata

3. Kotalanol, a Potent a-Glucosidase Inhibitor with Thiosugar Sulfonium Sulfate Structure, from Antidiabetic Ayurvedic Medicine Salacia reticulata.

4. Salaprionol and Ponkoranol with Thiosugar Sulfonium Sulfate Structure from Salacia prinoides and a-Glucosidase Inhibitory Activity of Ponkoranol and Kotalanol Desulfate

5. Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases

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