✦ LIBER ✦

NITROGEN FERTILIZATION AND THE FORMATION OF 2-PYRROLIDONE-5-CARBOXYLIC ACID IN STORED AND PROCESSED TABLE BEETS

✍ Scribed by C. Y. LEE; R. S. SHALLENBERGER; T. E. ACREE

Book ID: 108799454
Publisher: Institute of Food Technologists
Year: 2008
Tongue: English
Weight: 273 KB
Volume: 36
Category: Article
ISSN: 0022-1147
DOI: 10.1111/j.1365-2621.1971.tb03350.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

FORMATION OF 2-PYRROLIDONE-5-CARBOXYLIC

FORMATION OF 2-PYRROLIDONE-5-CARBOXYLIC ACID FROM GLUTAMINE DURING PROCESSING AND STORAGE OF SPINACH PUREE

✍ F. M. CLYDESDALE; Y. D. LIN; F. J. FRANCIS 📂 Article 📅 1972 🏛 Institute of Food Technologists 🌐 English ⚖ 375 KB

ChemInform Abstract: Chemoselectivity in

ChemInform Abstract: Chemoselectivity in the Intramolecular Aza-Wittig Reaction of N-[2-(Trisubstituted Phosphoranylidene)aminobenzoyl]-2-pyrrolidone-5-carboxylic Acid Derivatives.

✍ T. OKAWA; T. SUGIMORI; S. EGUCHI; A. KAKEHI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

Acid–base characterization of 5-hydroxyp

Acid–base characterization of 5-hydroxypyrazine-2-carboxylic acid and the role of ionic equilibria in the optimization of some process conditions for its biocatalytic production

✍ M. Sak-Bosnar; K. Kovar 📂 Article 📅 2005 🏛 Springer 🌐 English ⚖ 185 KB

A COMBINATION OF GLUTAMINASE AND pH CONT

A COMBINATION OF GLUTAMINASE AND pH CONTROL PREVENTS THE NONENZYMATIC CONVERSION OF l-GLUTAMINE INTO l-2-PYRROLIDINE-5-CARBOXYLIC ACID IN FOOD PROCESSING

✍ KAZUAKI YOSHIMUNE; TAKURO ABE; MITSUAKI MORIGUCHI 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 199 KB

On the Kolbe-Schmitt synthesis of pharma

On the Kolbe-Schmitt synthesis of pharmacologically useful salicylates: Carboxylation of 2,4-di-t-butylphenol and identification and reduction of the formation of 2,2′-dihydroxy-3,3′,5,5′-tetra-t-butylbiphenyl in the synthesis of 3,5-di-t-butylsalicylic acid

✍ Mankulathu V. Chidambaram; John R. J. Sorenson 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 290 KB

The initial yield of 3,5-di-t-butylsalicylic acid obtained via Kolbe-Schmitt carboxylation of the potassium salt of 2,4-di-t-butylphenol was less than 1% and was accompanied by a 65% yield of 2,2'-dihydroxy-3,3',5,5'- tetra-t-butylbiphenyl, a dimer of the 2,4-di-t-butylphenol formed by ortho couplin