The Exocyclic Olefin Geometry Control via Ireland–Claisen Rearrangement: Stereoselective Total Syntheses of Barmumycin and Limazepine E
Author:
Affiliation:
1. Latvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006, Riga, Latvia
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol4019453
Reference28 articles.
1. Isolation, Structural Assignment, and Total Synthesis of Barmumycin
2. Limazepines A−F, Pyrrolo[1,4]benzodiazepine Antibiotics from an Indonesian Micrococcus sp.
3. Pyrrolo[2,1-c][1,4]benzodiazepine as a Scaffold for the Design and Synthesis of Anti- Tumour Drugs
4. Total Syntheses of Prothracarcin and Tomaymycin by Use of Palladium Catalyzed Carbonylation
5. A versatile and efficient synthesis of carbinolamine-containing pyrrolo[1,4]benzodiazepines via the cyclization of N-(2-aminobenzoyl)pyrrolidine-2-carboxaldehyde diethyl thioacetals: total synthesis of prothracarcin
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