✦ LIBER ✦

BASE-CATALYZED CONDENSATION OF α-HALOGENATED KETONES WITH β-KETO ESTERS

✍ Scribed by DUNLOP, A. P.; HURD, CHARLES D.

Book ID: 120552869
Publisher: American Chemical Society
Year: 1950
Tongue: English
Weight: 292 KB
Volume: 15
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo01152a006

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Base-Catalyzed Condensations of Aldehyde

Base-Catalyzed Condensations of Aldehydes with α,β-Unsaturated Ketones 1

✍ Powell, Sargent G.; Wasserman, William J. 📂 Article 📅 1957 🏛 American Chemical Society 🌐 English ⚖ 703 KB

VCl3-Catalyzed Efficient Synthesis of β-

VCl3-Catalyzed Efficient Synthesis of β-Enamine Esters and Ketones from β-Keto Esters.

✍ Bavanthula Rajitha; Penthala Narsimha Reddy; Buridapad Sunil Kumar; Neeladri Sri 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 19 KB 👁 1 views

Lewis acid-catalyzed one-pot sequential

Lewis acid-catalyzed one-pot sequential reaction for the synthesis of α-halogenated β-keto esters

✍ Han-Feng Cui; Ke-Yan Dong; Jing Nie; Yan Zheng; Jun-An Ma 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 844 KB

Alkyl Carbonates in Synthetic Chemistry.

Alkyl Carbonates in Synthetic Chemistry. II. Condensation with Ketones. Synthesis of β-Keto Esters 1

✍ Wallingford, V. H.; Homeyer, August H.; Jones, David M. 📂 Article 📅 1941 🏛 American Chemical Society 🌐 English ⚖ 330 KB

Copper–bipyridine-catalyzed enantioselec

Copper–bipyridine-catalyzed enantioselective α-amination of β-keto esters

✍ Subrata Ghosh; Mecheril Valsan Nandakumar; Harald Krautscheid; Christoph Schneid 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 695 KB

Synthesis and cyclization reactions with

Synthesis and cyclization reactions with pyrazolopyrimidinyl keto esters part I. Reactivity of pyrazolopyrimidinylβ-keto ester and pyrazolopyrimidinylα,β-unsaturated ketones

✍ M. A. A. Awas 📂 Article 📅 2006 🏛 Versita 🌐 English ⚖ 271 KB

## Abstract 5-Acetyl-4,5-dihydro-1-phenylpyrazolo[3,4-d]pyrimidin-4-one was prepared and subjected to various chemical transformations to give novel 5-heterocyclic pyrazolopyrimidinone derivatives of expected important biological activity. Then, the latter compounds were used to obtain β-keto ester