ChemInform Abstract: FORMAL SYNTHESIS OF LAVENDAMYCIN METHYL ESTER: THE REGIOSELECTIVE SYNTHESIS TO THE BROMOQUINOLINEQUINONE SYSTEMS OF KEY INTERMEDIATE

Hibino, Satoshi; Okazaki, Miko; Ichikawa, Masataka; Sato, K.; Ishizu, Tomoko

doi:10.1002/chin.198527227

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

customersupport@researchsolutions.com

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

ChemInform Abstract: FORMAL SYNTHESIS OF LAVENDAMYCIN METHYL ESTER: THE REGIOSELECTIVE SYNTHESIS TO THE BROMOQUINOLINEQUINONE SYSTEMS OF KEY INTERMEDIATE

Abstract: Die Darstellung des bereits früher beschriebenen Brom‐chinolinchinons (VII) erfolgt nach dem angegebenen Schema.

Cited by 2 publications

References 1 publication

Diels–Alder Reactions of Heterocyclic Azadienes: Development of a Strategy for the Total Synthesis of Streptonigrin, Lavendamycin, and Synthetic Quinoline-5, 8-Quinones

Diels–Alder Reactions of Heterocyclic Azadienes: Development of a Strategy for the Total Synthesis of Streptonigrin, Lavendamycin, and Synthetic Quinoline-5, 8-Quinones

Iminophosphorane-mediated synthesis of 1-substituted-β-carbolines: investigative studies on the preparation of alkaloids lavendamycin and eudistomins framework.

Contact Info

Product

Resources

About