Synthesis of sphingofungin D and its stereoisomer at C-14
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Sphingofungins A,B,C, and d; a new family of antifungal agents. I. Fermentation, isolation, and biological activity.
2. Determination of the relative and absolute stereochemistry of sphingofungins A, B, C, and D
3. Synthesis of sphingosine relatives, XIV. A new synthesis of symbioramide, a Ca++-ATPase activator fromSymbiodinium sp.
4. Alkyne isomerization reagents: mixed alkali metal amides
5. The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
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1. The Alkyne Zipper Reaction: A Useful Tool in Synthetic Chemistry;Reactions;2022-12-30
2. A Modular Approach to the Antifungal Sphingofungin Family: Concise Total Synthesis of Sphingofungin A and C;Angewandte Chemie International Edition;2021-12-07
3. A Modular Approach to the Antifungal Sphingofungin Family: Concise Total Synthesis of Sphingofungin A and C;Angewandte Chemie;2021-12-07
4. Synthesis of β-Hydroxy-α,α-disubstituted Amino Acids through the Orthoamide-Type Overman Rearrangement of an α,β-Unsaturated Ester and Stereodivergent Intramolecular SN2′ Reaction: Development and Application to the Total Synthesis of Sphingofungin F;Bulletin of the Chemical Society of Japan;2018-04-15
5. Total Synthesis of Sphingofungin F by Orthoamide-Type Overman Rearrangement of an Unsaturated Ester;Organic Letters;2015-03-13
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