✦ LIBER ✦

Synthesis of 1-13C-1-indanone and 2-13C-1,2,3,4-tetrahydroquinoline

✍ Scribed by R. E. Pickering; M. A. Wysocki; E. J. Eisenbraun

Publisher: John Wiley and Sons
Year: 1985
Tongue: French
Weight: 229 KB
Volume: 22
Category: Article
ISSN: 0022-2135
DOI: 10.1002/jlcr.2580220811

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of 1,2,3,4-tetrahydronaphthale

Synthesis of 1,2,3,4-tetrahydronaphthalene-1-13C, naphthalene-1-13C, and 1-naphthalenol-1-13C

✍ R. E. Pickering; D. L. Bymaster; E. J. Eisenbraun 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 French ⚖ 233 KB

Synthesis of [1,2-13C]- and [2,3-13C]-la

Synthesis of [1,2-13C]- and [2,3-13C]-labeled δ-aminolevulinic acid

✍ Richard A. Bunce; Curtis L. Schilling III; Mario Rivera 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 French ⚖ 406 KB 👁 1 views

Synthesis of [2-13C, 2-14C]2-aminoethano

Synthesis of [2-13C, 2-14C]2-aminoethanol, [1-13C, 1-14C]2-chloroethylamine, N,N′-bis([1-13C, 1-14C]2-chloroethyl)-N-nitrosourea(BCNU) and N-([1-13C, 1-14C]2-chloroethyl)-N-nitrosourea(CNU)

✍ Ramani Narayan; Ching-Jer Chang 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 French ⚖ 311 KB

## Abstract [2‐^13^C, 2‐^14^C]2‐Aminoethanol hydrochloride was prepared in good yield from Na\*CN in a two step sequence by first converting the Na\*CN to OHCH~2~\*CN and then reducing the nitrile directly with a solution of borane‐tetrahydrofuran complex. The reaction procedure was simple and the

Synthesis of 2-amino-1,5-dihydro-1-(meth

Synthesis of 2-amino-1,5-dihydro-1-(methyl-13C)-4H-imidazol-4-one-5-13C (creatinine-13C2)

✍ A. Cohen; H. H. Hertz; R. Schaffer; M. M. Welch; E. White 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 French ⚖ 348 KB

ChemInform Abstract: Regioselective Synt

ChemInform Abstract: Regioselective Synthesis of 1,3,5-13C3 and 2,4-13C2-Labeled 2-Deoxyribonolactones.

✍ Paul J. Hatala; James Kallmerten; Philip N. Borer 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

Synthesis of [2-13C]phenol (1)

✍ Sun-Shine Yuan; Alfred M. Ajami 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 French ⚖ 221 KB

13 13 [2-C]cyclohexanone was synthesized through [ Clcyanation of cyclopentanone followed by acetylation, reduction and ring expansion. Treatment with cupric bromide/lithium bromide and dehydrobromination of the resulting labeled 1,6-dibromohexanone in a "one pot" procedure gave [2-13C]phenol.