The Structure and Stereochemistry of Gabosine K: Syntheses of 7-O-Acetylstreptol and 7-O-Acetyl-1-epi-streptol
Author:
Shing Tony,Cheng Hau
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Cited by
18 articles.
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1. Novel Stereoselective Syntheses of (+)-Streptol and (−)-1-epi-Streptol Starting from Naturally Abundant (−)-Shikimic Acid;ACS Omega;2021-06-23
2. Total Syntheses of (+)-Gabosine P, (+)-Gabosine Q, (+)-Gabosine E, (−)-Gabosine G, (−)-Gabosine I, (−)-Gabosine K, (+)-Streptol, and (−)-Uvamalol A by a Diversity-Oriented Approach Featuring Tunable Deprotection Manipulation;The Journal of Organic Chemistry;2017-03-20
3. Total syntheses of five uvacalols: structural validation of uvacalol A, uvacalol B and uvacalol C and disproval of the structures of uvacalol E and uvacalol G;Organic & Biomolecular Chemistry;2015
4. Total synthesis of 3-epi-(+)-lycoricidine from Garner aldehyde via intramolecular aldol cyclization;Tetrahedron Letters;2015-01
5. Toward synthesis of carbasugars (+)-gabosine C, (+)-COTC, (+)-pericosine B, and (+)-pericosine C;Carbohydrate Research;2014-03