✦ LIBER ✦

Chelation as a Driving Force in Organic Reactions. 1 A Generic Synthesis of Amino Acids by the Carboxylation and Alkylation of 3-Phenylhydantoin

✍ Scribed by Finkbeiner, Herman.

Book ID: 124088370
Publisher: American Chemical Society
Year: 1964
Tongue: English
Weight: 276 KB
Volume: 86
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja01059a071

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

CHELATION AS A DRIVING FORCE IN SYNTHESI

CHELATION AS A DRIVING FORCE IN SYNTHESIS. II. USE OF MAGNESIUM METHYL CARBONATE IN THE CARBOXYLATION AND ALKYLATION OF KETONES

✍ Stiles, Martin 📂 Article 📅 1959 🏛 American Chemical Society 🌐 English ⚖ 269 KB

Chelation as a Driving Force in Organic

Chelation as a Driving Force in Organic Reactions. V. 1 The Preparation of α-Nitro Esters through the Carboxylation of Nitroparaffins

✍ Finkbeiner, Herman L.; Wagner, George W. 📂 Article 📅 1963 🏛 American Chemical Society 🌐 English ⚖ 423 KB

Catalytic reaction of sylvan with alkyl

Catalytic reaction of sylvan with alkyl diazoacetates as a method for the synthesis of stereoisomeric 4-acetyl-1,3-butadiene-1-carboxylic acids

✍ O. M. Nefedov; L. E. Saltykova; A. E. Vasil'vitskii; V. M. Shostakovskii 📂 Article 📅 1986 🏛 Springer 🌐 English ⚖ 293 KB

A New General and Facile Method for the

A New General and Facile Method for the Synthesis of 4-Alkyl-1,3-oxazoline-4-carboxylic Acids from N-Acyl-2-alkylserines.

✍ Sebastian Olczyk; Janina E. Kaminska; Beata Kolesinska; Zbigniew J. Kaminski 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

A new synthesis of aziridine-2-carboxyla

A new synthesis of aziridine-2-carboxylates: Reaction of hexahydro-1,3,5-triazines or N-methoxymethylanilines with alkyl diazoacetates in the presence of lewis acid

✍ Hyun-Joon Ha; Jang-Min Suh; Kyung-Ho Kang; Young-Gil Ahn; Oksoo Han 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 474 KB

4b~t: Aziridine-2-carboxylates were prepared from the reaction of hexahydro-l,3,5-triazines or Nmethoxymethylanilines with alkyl diazeacetates in the presence of Lewis acid catalyst in high yield.

Inter- and Intramolecular Addition React

Inter- and Intramolecular Addition Reactions of Electron-Deficient Alkenes with Alkyl Radicals, Generated by SET-Photochemical Decarboxylation of Carboxylic Acids, Serve as a Mild and Efficient Method for the Preparation of γ-Amino Acids and Macrocyclic Lactones

✍ Yoshimi, Yasuharu; Masuda, Miho; Mizunashi, Tomoyuki; Nishikawa, Keisuke; Maeda, 📂 Article 📅 2009 🏛 American Chemical Society 🌐 English ⚖ 401 KB