✦ LIBER ✦

First stereoselective total synthesis of triumfettamide

✍ Scribed by Devi, Thongam Joymati; Saikia, Bishwajit; Barua, Nabin C.

Book ID: 121215043
Publisher: Elsevier Science
Year: 2013
Tongue: French
Weight: 395 KB
Volume: 69
Category: Article
ISSN: 0040-4020
DOI: 10.1016/j.tet.2013.08.068

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

First stereoselective total synthesis of

First stereoselective total synthesis of (+)-dodoneine

✍ P. Srihari; G. Rajendar; R. Srinivasa Rao; J.S. Yadav 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 164 KB

The first stereoselective total synthesis of the natural product (+)-dodoneine is described involving a Crimmins aldol reaction and a Horner-Wadsworth-Emmons olefination as the key steps.

First Stereoselective Total Synthesis of

First Stereoselective Total Synthesis of Oplopandiol

✍ Kumar Bejjanki, Naveen; Venkatesham, Akkaladevi; Balraju, Kammari; Nagaiah, Komm 📂 Article 📅 2013 🏛 John Wiley and Sons 🌐 German ⚖ 203 KB

First stereoselective total synthesis of

First stereoselective total synthesis of pectinolide A

✍ J.S. Yadav; S.S. Mandal 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 367 KB

First stereoselective total synthesis of

First stereoselective total synthesis of pectinolide H

✍ D. Ramesh; V. Shekhar; D. Chantibabu; S. Rajaram; U. Ramulu; Y. Venkateswarlu 📂 Article 📅 2012 🏛 Elsevier Science 🌐 French ⚖ 251 KB

First stereoselective total synthesis of

First stereoselective total synthesis of panaxjapyne C

✍ Pallavi Thakur; B. Kumaraswamy; G. Raji Reddy; Rakeshwar Bandichhor; K. Mukkanti 📂 Article 📅 2012 🏛 Elsevier Science 🌐 French ⚖ 510 KB

First stereoselective total synthesis of

First stereoselective total synthesis of Goniothalesdiol A

✍ J.S. Yadav; N. Rami Reddy; V. Harikrishna; B.V. Subba Reddy 📂 Article 📅 2009 🏛 Elsevier Science 🌐 French ⚖ 251 KB

The first total synthesis of Goniothalesdiol A, isolated from the stems of Goniothalamus amuyon (Annonaceae) is reported. The C2 stereocentre and C3/C4 syn diol were created by a Sharpless kinetic resolution followed by acetonide formation. The tetrahydropyran ring was formed and the C6 stereocentre