✦ LIBER ✦

Efficient Synthesis of Ningalin C.

✍ Scribed by Anucha Namsa-aid; Somsak Ruchirawat

Publisher: John Wiley and Sons
Year: 2010
Weight: 24 KB
Volume: 33
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200248204

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: First Total Synthes

ChemInform Abstract: First Total Synthesis of the Marine Alkaloids Purpurone (I) and Ningalin C (II).

✍ Christian Peschko; Wolfgang Steglich 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

An Efficient Synthesis of Semiplenamide

An Efficient Synthesis of Semiplenamide C.

✍ Iwan R. Davies; Matt Cheeseman; D. Gangani Niyadurupola; Steven D. Bull 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 19 KB 👁 1 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

ChemInform Abstract: A Total Synthesis o

ChemInform Abstract: A Total Synthesis of the Marine Alkaloid Ningalin B (I) from (S)-Proline.

✍ Katrin Hasse; Anthony C. Willis; Martin G. Banwell 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 12 KB 👁 2 views

Efficient Synthesis of New C-Functionali

Efficient Synthesis of New C-Functionalized Macrocyclic Polyamines

✍ Yoann Rousselin; Nicolas Sok; Frédéric Boschetti; Roger Guilard; Franck Denat 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 317 KB

An efficient synthesis of ethyne-1-13C

✍ Robert E. Colborn; K. Peter C. Vollhardt 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 French ⚖ 371 KB 👁 1 views

## Abstract A synthesis of the title compound from ^13^CO~2~ is described. The final step utilizes lithium hexamethyldisilazide as a base in the double dehydrobromination of 1,2‐dibromoethane‐1‐^13^C. Some alternative procedures are discussed.

An efficient synthesis of 1-[13C]-bromob

An efficient synthesis of 1-[13C]-bromobenze

✍ Christian Geletneky; Hartmut Balzer; Willi Bock; Stefan Berger 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 French ⚖ 225 KB 👁 1 views

Various routes to fbnctionalized benzenes labelled in position 1 were compared. 1-[ 13Cl-Bromobenzene has been synthesized in 7 steps with an overall yield of 5.4% from [ I 3C]-BaC03, by optimizing the direct transformation of p-nitrophenol into bromobenzene.