✦ LIBER ✦

Enantioselective Synthesis of (−)-Platensimycin Oxatetracyclic Core by Using an Intramolecular Diels−Alder Reaction

✍ Scribed by Ghosh, Arun K.; Xi, Kai

Book ID: 117990766
Publisher: American Chemical Society
Year: 2007
Tongue: English
Weight: 75 KB
Volume: 9
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol701783z

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Enantioselective Sy

ChemInform Abstract: Enantioselective Synthesis of (-)-Platensimycin Oxatetracyclic Core by Using an Intramolecular Diels—Alder Reaction.

✍ Arun K. Ghosh; Kai Xi 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 25 KB 👁 2 views

Enantioselective total synthesis of (−)-

Enantioselective total synthesis of (−)-equisetin using a Me3Al-mediated intramolecular Diels–Alder reaction

✍ Kumiko Yuki; Mitsuru Shindo; Kozo Shishido 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 84 KB

An efficient and enantioselective total synthesis of (-)-equisetin 1 has been accomplished using a diastereoselective Me 3 Al-mediated intramolecular Diels-Alder (IMDA) reaction as a key reaction step.

Synthesis of the decalin core of codinae

Synthesis of the decalin core of codinaeopsin via an intramolecular Diels–Alder reaction

✍ Ramanathan, Mani; Tan, Chun-Jui; Chang, Wen-Jung; Tsai, Hui-Hsu Gavin; Hou, Duen 📂 Article 📅 2013 🏛 Royal Society of Chemistry 🌐 English ⚖ 349 KB

Synthesis of the Tricyclic Core of Vinig

Synthesis of the Tricyclic Core of Vinigrol via an Intramolecular Diels−Alder Reaction

✍ Grisé,, Christiane M.; Tessier, Guillaume; Barriault, Louis 📂 Article 📅 2007 🏛 American Chemical Society 🌐 English ⚖ 103 KB

Intramolecular Diels-Alder reactions. 5

Intramolecular Diels-Alder reactions. 5 [1] Facile synthesis of an octahydrobenzocycloheptenone derivative utilising intramolecular Diels-Alder reaction

✍ Barbara Frey; Hans-Ulrich Reißig 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 52 KB 👁 2 views

Enantioselective synthesis and absolute

Enantioselective synthesis and absolute configuration of (−)-pulo'upone by asymmetric intramolecular diels-alder reaction

✍ Wolfgang Oppolzer; Dominique Dupuis; Giovanni Poli; Tony M. Raynham; Gérald Bern 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 297 KB

Pulo'upone (1) was synthesized via an asymmetric, bornane-10,2-sultam-directed, intramolecular Diels-Alderaction (2 -+ 2) and a 2\_pyridylcuprate/allylacetate coupling (18 + I). The (6'R, 9'S, 13'R. 14'R)configuration of (-)-I follows from an X-ray diffraction analysis of the cycloaddition product