✦ LIBER ✦

Synthesis of 4- cis -Phenyl- l -proline via Hydrogenolysis

✍ Scribed by Tamaki, Makoto; Han, Guoxia; Hruby, Victor J.

Book ID: 126005380
Publisher: American Chemical Society
Year: 2001
Tongue: English
Weight: 64 KB
Volume: 66
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo005625u

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of 4-cis-

ChemInform Abstract: Synthesis of 4-cis-Phenyl-L-proline via Hydrogenolysis.

✍ Makoto Tamaki; Guoxia Han; Victor J. Hruby 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

Synthesis of the cis and trans isomers o

Synthesis of the cis and trans isomers of 4-Chloro-L-proline, 4-Bromo-L-proline, and 4-Amino-L-proline

✍ Andreatta, RH; Nair, V; Robertson, AV; Simpson, WRJ 📂 Article 📅 1967 🏛 Commonwealth Scientific and Industrial Research Or 🌐 English ⚖ 952 KB

Synthesis of 4-Oxo-L-proline and cis-4-H

Synthesis of 4-Oxo-L-proline and cis-4-Hydroxy-L-proline Derivatives from L-Aspartic Acid

✍ Prof. Dr. Klaus Burger; Dr. Martin Rudolph; Dipl.-Chem. Susanna Fehn 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 420 KB 👁 2 views

Practical Synthesis of Boc-Protected cis

Practical Synthesis of Boc-Protected cis -4-Trifluoromethyl and cis -4-Difluoromethyl- l - prolines

✍ Qiu, Xiao-long; Qing, Feng-ling 📂 Article 📅 2002 🏛 American Chemical Society 🌐 English ⚖ 62 KB

Synthesis of cis- and trans-4-mercapto-L

Synthesis of cis- and trans-4-mercapto-L-proline derivatives

✍ Verbiscar, Anthony J.; Witkop, Bernhard. 📂 Article 📅 1970 🏛 American Chemical Society 🌐 English ⚖ 522 KB

Facile synthesis of (+)-α-allokainic aci

Facile synthesis of (+)-α-allokainic acid via Pd-catalyzed hydrogenolysis of allyl acetate derived from trans-4-hydroxy-l-proline

✍ Dawei Ma; Wengen Wu; Ping Deng 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 63 KB

Pd(PPh 3 ) 4 /PPh 3 -catalyzed hydrogenolysis of 3a derived from trans-4-hydroxy-L-proline using ammonium formate as a hydride reagent, provides olefin 4 as a major product, which is hydrolyzed to give (+)-a-allokainic acid.