✦ LIBER ✦

Expeditious enantioselective syntheses of indole alkaloids of Aspidosperma- and Hunteria-type

✍ Scribed by Node, Manabu; Nagasawa, Hideko; Fuji, Kaoru

Book ID: 127356204
Publisher: American Chemical Society
Year: 1987
Tongue: English
Weight: 414 KB
Volume: 109
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja00259a060

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Chiral total synthesis of indole alkaloi

Chiral total synthesis of indole alkaloids of the Aspidosperma and Hunteria types

✍ Node, Manabu; Nagasawa, Hideko; Fuji, Kaoru 📂 Article 📅 1990 🏛 American Chemical Society 🌐 English ⚖ 733 KB

ChemInform Abstract: Asymmetric Synthesi

ChemInform Abstract: Asymmetric Synthesis of Key Synthetic Intermediates of Aspidosperma and Hunteria Type Indole Alkaloids.

✍ K. OKADA; K. MURAKAMI; H. TANINO; H. KAKOI; S. INOUE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB

Synthesis of analogues of hunteria and a

Synthesis of analogues of hunteria and aspidosperma alkaloids from a common intermediate

✍ J.E.D. Barton; John Harley-Mason; K.C. Yates 📂 Article 📅 1965 🏛 Elsevier Science 🌐 French ⚖ 151 KB

General methods of synthesis of indole a

General methods of synthesis of indole alkaloids. VII. Syntheses of dl-dihydrogambirtannine and aspidosperma-strychnos alkaloid models

✍ Wenkert, Ernest.; Dave, K. G.; Gnewuch, C. T.; Sprague, P. W. 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 776 KB

Biosynthesis of Indole Alkaloids. The As

Biosynthesis of Indole Alkaloids. The Aspidosperma and Iboga Bases

✍ Wenkert, Ernest. 📂 Article 📅 1962 🏛 American Chemical Society 🌐 English ⚖ 540 KB

Enantioselective syntheses of the indole

Enantioselective syntheses of the indole alkaloid (+)-R-decarbomethoxytetrahydrosecodine and its enantiomer

✍ Mercedes Amat; Grigorii Pshenichnyi; Joan Bosch; Elies Molins; Carles Miravitlle 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 240 KB

The alkaloid (+)-R-decarbomethoxytetrahydrosecodine (+)-1 has been synthesized by alkylation of (R)-3-ethylpiperidine with 3-(2-bromoethyl)-2ethylindole (7). The required enantiopurc piperidine was prepared by alkylation of the chiral non-racemic oxazolopiperidone (+)-trttns-.8 followed by reduction