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New Route to the Ergoline Skeleton via Cyclization of 4-Unsubstituted Indoles

โœ Scribed by Burley, Scott D.; Lam, Vicky V.; Lakner, Frederick J.; Bergdahl, B. Mikael; Parker, Matthew A.


Book ID
120340822
Publisher
American Chemical Society
Year
2013
Tongue
English
Weight
283 KB
Volume
15
Category
Article
ISSN
1523-7060

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๐Ÿ“œ SIMILAR VOLUMES


Chemistry of indoles carrying a basic fu
โœ Mรกria Incze; Istvรกn Moldvai; Eszter Temesvรกri-Major; Gรกbor Dรถrnyei; Mรกria Kajtรกr ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 198 KB

Starting from N-pivaloyl-Uhle's ketone a new synthetic approach to the ergoline skeleton has been elaborated. Ring D of the tetracyclic skeleton was formed by an intramolecular Dieckmann-condensation of a diester, obtained in a Reformatsky reaction of a properly substituted derivative of N-pivaloyl

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โœ O. B. Smirnova; T. V. Golovko; L. M. Alekseeva; A. S. Shashkov; V. G. Granik ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 67 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โ€œFull Textโ€ option. The original article is trackable v