✦ LIBER ✦

[2+2+2] Cycloadditions of Alkynylynamides – A Total Synthesis of Perlolyrine and the First Total Synthesis of “Isoperlolyrine”

✍ Scribed by Benjamin Dassonneville; Bernhard Witulski; Heiner Detert

Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 475 KB
Volume: 2011
Category: Article
ISSN: 1434-193X
DOI: 10.1002/ejoc.201100121

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

First Total Synthesis of (-)-AL-2.

✍ Naoki Miyakoshi; Chisato Mukai 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 55 KB 👁 1 views

Total Synthesis of Lavendamycin by a [2+

Total Synthesis of Lavendamycin by a [2+2+2] Cycloaddition

✍ Felix Nissen; Heiner Detert 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 629 KB

A First Total Synthesis of Ganglioside H

A First Total Synthesis of Ganglioside HLG-2

✍ Yuki Iwayama; Hiromune Ando; Hideharu Ishida; Makoto Kiso 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 410 KB 👁 1 views

First Total Synthesis of J2 Isoprostane.

✍ Giuseppe Zanoni; Alessio Porta; Francesca Castronovo; Giovanni Vidari 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 58 KB 👁 1 views

The First Stereoselective Total Synthesi

The First Stereoselective Total Synthesis of Lankanolide. Part 2.

✍ Tatsuo Hamada; Yukinari Kobayashi 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 49 KB 👁 1 views

Total Synthesis of (±)-2-Pupukeanone

✍ Georg Fráter; Jean Wenger 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 German ⚖ 338 KB

## Abstract (±)‐2‐Pupukenone (**4**) has been synthesized, the key step being the intramolcular __Diels‐Alder__ reaction of the intermediate **13** to **14** (42%) and **15** (14%). The bromodiene **12** has been obtained from the reaction of α‐isopropylidene‐γ‐lactone (__Scheme 2__) **12** with so