๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Chiral dihydropyridones as synthetic intermediates. Asymmetric synthesis of (+)-elaeokanine A and (+)-elaeokanine C

โœ Scribed by Comins, Daniel L.; Hong, Hao


Book ID
121492314
Publisher
American Chemical Society
Year
1991
Tongue
English
Weight
271 KB
Volume
113
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Elaeocarpus Alkaloids. The Synthesis of
โœ Joseph J. Tufariello; Sk.Asrof Ali ๐Ÿ“‚ Article ๐Ÿ“… 1979 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 199 KB

The synthesis of dl-elaeokanine-A and dl-elaeokanine-C is described by an approach which utilizes a nitrone cycloaddition to generate a B-aminoketone, which upon annulation produces one or the other of the title alkaloids depending upon conditions. We wish to describe herein a synthetic entry into t

Enantiopure N-acyldihydropyridones as sy
โœ Daniel L. Comins; Nezha Radi Benjelloun ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 259 KB

The trans-pip&dine alkaloid, (-)-solenopsin A. was prepared in seven steps from readily available 4-~haxy-3\_(niiropropyrsilyllpyrfdin in 43% overall yield. The addition of organ~tallics to chiral 1-acylpyridinium salt 1 gives N-acyl-2-alkyl-23&hydta~4pyridones 2 with high diastereoselectivity.\*~ T