✦ LIBER ✦

Reaction of organolead triacetates with 4-ethoxycarbonyl-2-methyloxazol-5-one. The synthesis of α-aryl and α-vinyl N-acetylglycine ethyl esters and their enzymic resolution

✍ Scribed by Jacqueline Morgan; John T. Pinhey

Book ID: 103401182
Publisher: Elsevier Science
Year: 1994
Tongue: French
Weight: 271 KB
Volume: 35
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(94)88529-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reaction of organolead triacetates with

Reaction of organolead triacetates with 4-ethoxycarbonyl-2-methyl-4,5-dihydro-1,3-oxazol-5-one. The synthesis of α-aryl- and α-vinyl-N-acetylglycines and their ethyl esters and their enzymic resolution

✍ Morgan, Jacqueline; Pinhey, John T.; Sherry, Christopher J. 📂 Article 📅 1997 🏛 Royal Society of Chemistry ⚖ 509 KB

ChemInform Abstract: Reaction of Organol

ChemInform Abstract: Reaction of Organolead Triacetates with 4-Ethoxycarbonyl-2-methyl-4,5- dihydro-1,3-oxazol-5-one. The synthesis of α-Aryl- and α- Vinyl-N-acetylglycines and Their Ethyl Esters and Their Enzymic Resolution.

✍ J. MORGAN; J. T. PINHEY; C. J. SHERRY 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 2 views

Synthesis of Heterocyclic Compounds Usin

Synthesis of Heterocyclic Compounds Using Amidines as Their Ene-1,1-diamine Tautomers. Part 1. Synthesis of 4,5-Dihydro-3H-pyridin-2-one, 3,4-Dihydropyrrol-2-one and 1,3-Dihydropyrrol-2-one Derivatives by the Reaction of Amidines with α,β-Unsaturated Esters.

✍ Kunio Ito; Yoshiko Kizuka; Yuji Hirano 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

Synthesis of heterocyclic compounds usin

Synthesis of heterocyclic compounds using amidines as their ene-1,1-diamine tautomers. I. Synthesis of 4,5-dihydro-3H-pyridin-2-one, 3,4-dihydropyrrol-2-one and 1,3-dihydropyrrol-2-one derivatives by the reaction of amidines with α,β-unsaturated esters

✍ Kunio Ito; Yoshiko Kizuka; Yuji Hirano 📂 Article 📅 2005 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 82 KB 👁 1 views

N-t-Butylacetamidines 1 on heating with methyl acrylate (2) at 200˚ gave the 4,5-dihydro-3H-pyridin-2one derivatives 5. Michael addition of the acetamidines 1 as their ene-1,1-diamine tautomers 1' to 2 and the subsequent cyclization of the adducts gave derivatives 5. Amidines 1 on reaction with trim