✦ LIBER ✦

Novel regioselective hydroxylations of pyridine carboxylic acids at position C2 and pyrazine carboxylic acids at position C3

✍ Scribed by A. Tinschert; A. Tschech; K. Heinzmann; A. Kiener

Book ID: 105954006
Publisher: Springer
Year: 2000
Tongue: English
Weight: 299 KB
Volume: 53
Category: Article
ISSN: 1432-0614
DOI: 10.1007/s002530050007

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of short chain carboxylic acid

Synthesis of short chain carboxylic acids labelled with 13C and 2H at various positions

✍ Bruce H. Baretz; Charles P. Lollo; Kay Tanaka 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 French ⚖ 412 KB

ChemInform Abstract: Epimerization of tr

ChemInform Abstract: Epimerization of trans-3-Arylaziridine-2-carboxylates at the C3 Position.

✍ Takuya Kumamoto; Shin-ichiro Nagayama; Yukiko Hayashi; Hiroaki Kojima; Lemin Dav 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 23 KB 👁 2 views

Acid catalysis in the formation of dioxo

Acid catalysis in the formation of dioxopiperazines from peptides containing tetrahydroisoquinoline-3-carboxylic acid at position 2

✍ CAPASSO, SANTE ;SICA, FILOMENA ;MAZZARELLA, LELIO ;BALBONI, GIANFRANCO ;GUERRINI 📂 Article 📅 2009 🏛 Wiley (Blackwell Publishing) 🌐 English ⚖ 577 KB

Synthesis of 7-Hydroxy-4,5,6,7-tetrahydr

Synthesis of 7-Hydroxy-4,5,6,7-tetrahydrothieno[3,2-c]pyridine-6-carboxylic Acids and 4-Hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic Acids

✍ Maffrand, Jean-Pierre; Sola, R使ine; Frehel, Daniel; Brugidou, Jean 📂 Article 📅 1982 🏛 Japan Institute of Heterocyclic Chemistry 🌐 English ⚖ 88 KB

Isolation of new 6-methylnicotinic-acid-

Isolation of new 6-methylnicotinic-acid-degrading bacteria, one of which catalyses the regioselective hydroxylation of nicotinic acid at position C2

✍ Andreas Tinschert; Andreas Kiener; Klaus Heinzmann; A. Tschech 📂 Article 📅 1997 🏛 Springer 🌐 English ⚖ 132 KB

A novel synthesis of carboxylic acid der

A novel synthesis of carboxylic acid derivatives having a quaternary carbon at 3-position and functional groups at 4-position from 1-chlorovinyl p-tolyl sulfoxides and acetic acid esters

✍ Tsuyoshi Satoh; Shimpei Sugiyama; Hiroyuki Ota 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 112 KB

Addition of the lithium enolate of acetic acid esters to 1-chlorovinyl p-tolyl sulfoxides, which were derived from ketones and chloromethyl p-tolyl sulfoxide in three steps in good yields, gave carboxylic acid esters having a quaternary carbon at the 3-position, and chlorine and sulfinyl groups at t