✦ LIBER ✦

Enzymatic conversion of homoisocitric acid into α-ketoadipic acid

✍ Scribed by Murray Strassman; Louis N. Ceci; Bonnie E. Silverman

Book ID: 118848883
Publisher: Elsevier Science
Year: 1964
Tongue: English
Weight: 180 KB
Volume: 14
Category: Article
ISSN: 0006-291X
DOI: 10.1016/0006-291x(64)90447-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ON THE PREPARATION OF α-KETOADIPIC ACID

✍ Nelson, Randall B.; Gribble, Gordon W. 📂 Article 📅 1973 🏛 Taylor and Francis Group 🌐 English ⚖ 140 KB

Inactivation of α-ketoglutarate dehydrog

Inactivation of α-ketoglutarate dehydrogenase during oxidative decarboxylation of α-ketoadipic acid

✍ V.I. Bunik; O.G. Pavlova 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 489 KB

Syntheses of (−)-Isocitric Acid Lactone

Syntheses of (−)-Isocitric Acid Lactone and (−)-Homoisocitric Acid. A New Method of Conversion of Alkynylsilanes into the Alkynyl Thioether and Corresponding Carboxylic Acids

✍ Schmitz, Carole; Rouanet-Dreyfuss, Anne-Claire; Tueni, Marie; Biellmann, Jean-Fr 📂 Article 📅 1996 🏛 American Chemical Society 🌐 English ⚖ 275 KB

Enzymatic Conversion of All-cis-Polyunsa

Enzymatic Conversion of All-cis-Polyunsaturated Fatty Acids into Prostaglandins

✍ VAN DORP, D. A.; BEERTHUIS, R. K.; NUGTEREN, D. H.; VONKEMAN, H. 📂 Article 📅 1964 🏛 Nature Publishing Group 🌐 English ⚖ 318 KB

ChemInform Abstract: Syntheses of (-)-Is

ChemInform Abstract: Syntheses of (-)-Isocitric Acid Lactone and (-)-Homoisocitric Acid. A New Method of Conversion of Alkynylsilanes into the Alkynyl Thioether and Corresponding Carboxylic Acids.

✍ C. SCHMITZ; A.-C. ROUANET-DREYFUSS; M. TUENI; J.-F. BIELLMANN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB

Conversion of thiolesters of α,β-unsatur

Conversion of thiolesters of α,β-unsaturated acids into the free acids

✍ L. B. Bos; J. F. Arens 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 530 KB

## Abstract Ethanethiolesters can be converted into free acids by: treatment with a mixture of mercuric chloride and mercuric oxide in aqueous acetone (table I), treatment with benzaldehyde and boron trifluoride in chloroform (table II). The latter procedure probably involves the reactions (1)‐(4