Synthesis of Maremycins A and D1 via Cycloaddition of a Nitrone with (E)-3-Ethylidene-1-methylindolin-2-one
Author:
Affiliation:
1. Showa Pharmaceutical University, 3-3165 Higashi-tamagawagakuen, Machida, Tokyo 194-8543, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol800515w
Reference31 articles.
1. Marine bacteria, VIII. Maremycin A and B, new diketopiperazines from a marineStreptomyces sp.
2. Maremycins C and D, New Diketopiperazines, and Maremycins E and F, Novel Polycyclicspiro-Indole Metabolites Isolated fromStreptomycessp.
3. Microwave mediated synthesis of spiro-(indoline-isoxazolidines): mechanistic study and biological activity evaluation
4. To our knowledge, this is the only report that refers to cycloaddition of a nitrone with an indolyl-3-ylidene-2-one compound.
5. Oxindole alkaloids. A novel non-biomimetic entry to (−)-Horsfiline.
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