✦ LIBER ✦

Synthesis of 14C-labeled 5-[1-hydroxy-2-[2-(o-methoxyphenoxy) ethylamino] ethyl]-2-methylbenzenesulfonamide hydrochloride (YM-09538)

✍ Scribed by Hideki Arima; Kazuharu Tamazawa

Publisher: John Wiley and Sons
Year: 1983
Tongue: French
Weight: 280 KB
Volume: 20
Category: Article
ISSN: 0022-2135
DOI: 10.1002/jlcr.2580200705

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of 14C-labeled pramiracetam hy

Synthesis of 14C-labeled pramiracetam hydrochloride, N-[2-(bis[1-methylethyl]amino)ethyl]-2-oxo-1-pyrrolidine-acetamide-α-14C hydrochloride, CI-879 hydrochloride

✍ Jon D. Hartman; C. C. Huang; D. E. Butler 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 French ⚖ 221 KB

Synthesis of I4C-Labeled Pramiracetam Hydrochloride, E-[2-(Bis[ 1-me thyle thyl 1 aminole thyl ] -2-0x0-l -p y r r o l i d i n eac.etamide-a-14C Hydrochloride, CI-879 Hydrochloride1

Synthesis of 14C-labelled 3-(1-hydroxy-2

Synthesis of 14C-labelled 3-(1-hydroxy-2-piperidinoethyl)-5-phenylisoxazole citrate (31252-S)

✍ H. Minato; T. Nagasaki; T. Yokoshima; K. Suga; M. Yamaguchi 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 French ⚖ 268 KB

## Abstract 3‐(1‐Hydroxy‐2‐piperidinoethyl)‐5‐phenylisoxazole citrate, 31252‐S (I) has been labelled with carbon‐14. The carbon‐14 label was incorporated into the C‐2 position of the side‐chain to give (II) and into the C‐4 position of the isoxazole ring of the molecule to give (III). The carbon‐1

Synthesis of 14C- and 2H-labeled (3S)-1-

Synthesis of 14C- and 2H-labeled (3S)-1-benzyl-3-pyrrolidinyl methyl (4S)-2,6-dimethyl-4-(m-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate hydrochloride (YM-09730-5), a potent calcium antagonist

✍ Hideki Arima; Kazuharu Tamazawa; Makoto Takeuchi 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 French ⚖ 343 KB

Synthesis and 5-HT2A, 5-HT1A and α1-Bind

Synthesis and 5-HT2A, 5-HT1A and α1-Binding Affinities of 2-[2-Hydroxy-3-(pyridin-3-yl-methyl)amino]-, 2-[2-Hydroxy-3-(2-pyridin-2-yl-ethyl)amino]- and 2-[2-Hydroxy-3-(4-N-methyl-piperazin-1-yl)-amino]propoxybenzaldehyde-O-(substituted) Benzyl Oximes

✍ Elisabetta Orlandini; Simona Rapposelli; Susanna Nencetti; Gino Giannaccini; Lau 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 288 KB 👁 1 views

Synthesis of [carbonyl-14C]- and (methox

Synthesis of [carbonyl-14C]- and (methoxy-d3)-labeled N-[(2RS, 3RS)-1-benzyl-2-methyl-3-pyrrolidinyl] −5-chloro-2-methoxy-4-(methylamino) benzamide (YM-09151-2). A new potent neuroleptic agent

✍ Kazuharu Tamazawa; Hideki Arima 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 French ⚖ 485 KB

## Abstract A new potent neuroleptic agent YM‐09151‐2, N‐[(2RS, 3RS)‐1‐benzyl‐2‐methyl‐3‐pyrrolidinyl]‐5‐chloro‐2‐methoxy‐4‐ (methylamino) benzamide (**10c**), was labeled with carbon‐14 and deuterium for biochemical studies such as metabolism and 14 pharmacokinetics. The synthesis of [carbonyl‐^14

4-Hydroxyquinolones-2. Part 91. Synthesi

4-Hydroxyquinolones-2. Part 91. Synthesis and Properties of Ethyl 1-Substituted- 4-hydroxy-6-methyl-2-oxo-dihydropyridine-5-carboxylates.

✍ I. V. Ukrainets; L. V. Sidorenko; O. V. Gorokhova; O. V. Shiskhin 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 16 KB 👁 1 views