✦ LIBER ✦

An improved stereoselective total synthesis of (R)-rugulactone

✍ Scribed by Abhishek Goswami; Partha Pratim Saikia; Bishwajit Saikia; Devdutt Chaturvedi; Nabin C. Barua

Book ID: 113929795
Publisher: Elsevier Science
Year: 2011
Tongue: French
Weight: 253 KB
Volume: 52
Category: Article
ISSN: 0040-4039
DOI: 10.1016/j.tetlet.2011.07.109

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Stereoselective Total Synthesis of Rugul

Stereoselective Total Synthesis of Rugulactone

✍ Biswanath Das; Yallamalla Srinivas; Chithaluri Sudhakar; Parigi Raghavendar Redd 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 German ⚖ 163 KB

## Abstract The stereoselective synthesis of the naturally occurring dihydropyranone rugulactone has been accomplished starting from 3‐phenylpropan‐1‐ol employing __Maruoka__ allylation and ring‐closing metathesis as the key steps.

Stereoselective Synthesis of Both Enanti

Stereoselective Synthesis of Both Enantiomers of Rugulactone

✍ Böse, Dietrich; Fernández, Enrique; Pietruszka, Jörg 📂 Article 📅 2011 🏛 American Chemical Society 🌐 English ⚖ 989 KB

An Improved Stereoselective Synthesis of

An Improved Stereoselective Synthesis of L-Alanosine

✍ Paolo Strazzolini; Maria Grazia Dall’Arche; Maura Zossi; Andrea Pavsler 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 139 KB

Stereoselective total synthesis of (+-)-

Stereoselective total synthesis of (+-)-fukinone

✍ Piers, Edward.; Smillie, R. Dean. 📂 Article 📅 1970 🏛 American Chemical Society 🌐 English ⚖ 476 KB

Stereoselective Total Synthesis of (+)-C

Stereoselective Total Synthesis of (+)-Cardiobutanolide

✍ Prasad, Kavirayani R.; Gholap, Shivajirao L. 📂 Article 📅 2008 🏛 American Chemical Society 🌐 English ⚖ 98 KB

Stereoselective total synthesis of (+)-a

Stereoselective total synthesis of (+)-artemisinin

✍ J.S Yadav; R Satheesh Babu; G Sabitha 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 163 KB

The total synthesis of the novel antimalarial drug, a sesquiterpene endoperoxide, (+)-artemisinin is described. The approach is flexible and stereoselective. The use of an intermolecular radical reaction on an intermediate iodolactone and a Wittig reaction on a ketone were employed for the synthesis