ChemInform Abstract: Acetogenic Isoquinoline Alkaloids. Part 138. Jozipeltine A, a Novel, Unnatural Dimer of the Highly Hydroxylated Naphthylisoquinoline Alkaloid Dioncopeltine A.
β Scribed by Gerhard Bringmann; Wael Saeb; Michael Wohlfarth; Kim Messer; Reto Brun
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ Synopsis
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 βFull Textβ option. The original article is trackable via the βReferencesβ option.
π SIMILAR VOLUMES
Acetogenic Isoquinoline Alkaloids. Part 120. Directed Joint Total Synthesis of the Three Naphthylisoquinoline Alkaloids Dioncolactone A, Dioncopeltine A, and 5'-O-Demethyldioncophylline A. -The first total synthesis of three title naphthylisoquinoline alkaloids dioncolactone A (VI), dioncopeltine A
Acetogenic Isoquinoline Alkaloids. Part 88. Antiprotozoal Activity of Naphthylisoquinoline Alkaloids. Part 7. Synthesis of Pindikamine A, a Michellamine-Related Dimer of a Non-Natural, "Skew" Naphthylisoquinoline. -The first preparation of a non-natural (skew, since 6,8'-coupled) naphthylisoquinoli
Acetogenic Isoquinoline Alkaloids. Part 105. First Synthesis of the Antimalarial Naphthylisoquinoline Alkaloid Dioncophylline C, and Its Unnatural Anti-HIV Dimer, Jozimine C. -The key steps in the synthesis of the title alkaloid (VII) are cyclization of the bromide (IV) and subsequent reductive rin
Acetogenic Isoquinoline Alkaloids. Part 117. First Total Synthesis of Dioncophylline B, a 7,6'-Coupled Naphthylisoquinoline Alkaloid. -The title compound is synthesized by a crucial biaryl coupling of the appropriately functionalized naphthalene (I) and the isoquinoline (II) with Mom-protected oxyg