✦ LIBER ✦

Synthesis of potential anticonvulsants: Condensation of isatins with acetone and related ketones

✍ Scribed by F. D. Popp; R. Parson; B. E. Donigan

Publisher: John Wiley and Sons
Year: 1980
Tongue: English
Weight: 257 KB
Volume: 69
Category: Article
ISSN: 0022-3549
DOI: 10.1002/jps.2600691035

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Potential anticonvulsants VI: Condensati

Potential anticonvulsants VI: Condensation of isatins with cyclohexanone and other cyclic ketones

✍ Hossein Pajouhesh; Randy Parson; Frank D. Popp 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 English ⚖ 298 KB

Potential anticonvulsants IV: Condensati

Potential anticonvulsants IV: Condensation of isatin with benzoylacetone and isopropyl methyl ketone

✍ Frank D. Popp; Hossein Pajouhesh 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 236 KB

L-Proline-Catalyzed Asymmetric Aldol Con

L-Proline-Catalyzed Asymmetric Aldol Condensation of N-Substituted Isatins with Acetone.

✍ Gang Chen; Ye Wang; Hongping He; Suo Gao; Xiaosheng Yang; Xiaojiang Hao 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 21 KB

Synthesis of β-Thioxo Ketones by Condens

Synthesis of β-Thioxo Ketones by Condensation of Ketones with Thionic Esters

✍ Doz. Dr. E. Uhlemann; Dipl.-Chem. Helmut Müler 📂 Article 📅 1965 🏛 John Wiley and Sons 🌐 English ⚖ 113 KB

ChemInform Abstract: Synthesis and Struc

ChemInform Abstract: Synthesis and Structure—Activity Relationships of Potential Anticonvulsants Based on 2-Piperidinecarboxylic Acid and Related Pharmacophores.

✍ Bin Ho; A. Michael Crider; James P. Stables 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

Mixed Aromatic Acyloin Condensations wit

Mixed Aromatic Acyloin Condensations with Recombinant Benzaldehyde Lyase: Synthesis of α-Hydroxydihydrochalcones and Related α-Hydroxy Ketones

✍ Monica Sanchez-Gonzalez; John P. N. Rosazza 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 101 KB

## Abstract Recombinant benzaldehyde lyase (BAL), expressed and purified from __E. coli__ strain JM‐109, was used to catalyze the condensation of a series of methoxybenzaldehydes and phenylacetaldehyde in the synthesis of α‐(__R__)‐hydroxydihydrochalcones. Enantiomerically pure 1‐hydroxy‐1,3‐diphen