𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of Aristotelia-Type Alkaloids. Part XIII. Total syntheses of (+)-makonine, (+)-aristotelinone, and (+)-11,12-didehydroaristoteline

✍ Scribed by Reto Stahl; Renato Galli; Rolf Güller; Hans-Jürg Borschberg


Publisher
John Wiley and Sons
Year
1994
Tongue
German
Weight
509 KB
Volume
77
Category
Article
ISSN
0018-019X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of Aristotelia-Type Alkaloids.
✍ Markus Dobler; James C. Anderson; Mathias Juch; Hans-Jürg Borschberg 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 German ⚖ 565 KB

Synthetic (+)-makomakine (6) was transformed in six steps into (+)-( 17 R,18R)-17,18-dihydrohobartine-17,18-diol((+)-5) with an overall yield of 38 % (Scheme 2). This compound was shown to be identical with natural hobartinol, a monoterpene indole alkaloid from Aristoteliu uustrulusicu, originally b

Synthesis of Aristotelia-Type Alkaloids,
✍ Renato Galli; Markus Dobler; Rolf Güller; Reto Stahl; Hans-Jürg Borschberg 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 German ⚖ 182 KB

Dedicated to Professor Dieter Seebach on the occasion of his 65th birthday Two independent total syntheses of the Aristotelia alkaloid (À)-serratenone ((À)-1) are disclosed, one starting with (À)-a-pinene, the other one with (S)-a-terpineol. These correlations led to a revision of the originally pro

ChemInform Abstract: Syntheses of Strych
✍ Martin E. Kuehne; Feng Xu 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB

Syntheses of Strychnan-and Aspidospermatan-Type Alkaloids. Part 11. Total Syntheses of (-)-Lochneridine and (-)-and Racemic 20-epi-Lochneridine. -The methods presented in the preceding article for the synthesis of strychnine are modified to prepare the title alkaloids. Pentacyclic ketone (I) forms