✦ LIBER ✦

Synthesis of N-substituted pyrroles from 1-R-3-R1-3,4-dichlorobutanones

✍ Scribed by é. I. Mamedov; A. G. Ismailov; V. G. Ibragimov; G. M. Bairamov

Publisher: Springer US
Year: 1990
Tongue: English
Weight: 326 KB
Volume: 26
Category: Article
ISSN: 0009-3122
DOI: 10.1007/bf00472476

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of 4-R-3-

ChemInform Abstract: Synthesis of 4-R-3-(4-R1-5-R2-1,2,3-Triazol-1-yl)furazans. Part 1. Azidofurazans in 1,3-Dipolar Cycloaddition Reactions with Substituted Acetylenes.

✍ L. V. Batog; L. S. Konstantinova; V. Yu. Rozhkov; Yu. A. Strelenko; O. V. Lebede 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

Synthesis and transformations of (1R,2R,

Synthesis and transformations of (1R,2R,3S,4R)-4-O-benzylhydroxylamino-2,3-O-isopropylidene-1,2,3-cyclopentanetriol: synthesis of (1S,2R,3S,4R)-4-amino-2,3-O-isopropylidene-1,2,3-cyclopentanetriol

✍ José Marco-Contelles; Ma.Mercedes Rodríguez-Fernández 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 533 KB

## Synthesis and transformations of (1R,2R,3S,4R)-4-O- benzylhydroxylamino-2,3-O-isopropylidene-1,2,3-cyclopentanetrioh synthesis of (1S,2R,3S,4R)-4-amino-2,3-O-isopropylidene-l,2,3cyclopentanetriol

Synthesis of (1S,3R,4R,5R)-3,4-(isopropy

Synthesis of (1S,3R,4R,5R)-3,4-(isopropylidenedioxy)-1-[(1R)-1,2-(isopropylidenedioxy)ethyl]-2-oxaspiro[4.4]non-6-en-8-one from d-glucose

✍ Kin-ichi Tadano; Satoshi Kanazawa; Hirohiko Yamada; Seiichiro Ogawa 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 352 KB

ChemInform Abstract: Synthesis of 1′-Aza

ChemInform Abstract: Synthesis of 1′-Aza-C-nucleosides from (3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol.

✍ Vyacheslav V. Filichev; Erik B. Pedersen 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

Preparation of carbon-14 labeled (3R)-7-

Preparation of carbon-14 labeled (3R)-7-hydroxy-N-(1S)-1-{[(3R,4R)-4-(3-hydroxyphenyl)-3,4-dimethyl-1-piperidinyl]methyl}-2-methylpropyl-1,2,3,4-tetrahydroisoquinolinecarboxamide (JDTic)

✍ Bertold D. Berrang; Anita H. Lewin; F. Ivy Carroll 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 French ⚖ 128 KB 👁 1 views

## Abstract Starting with [^14^C]‐D‐tyrosine, carbon‐14 labeled JDTic dihydrochloride with specific activity 15 mCi/mol was prepared in 5% radiochemical yield. Separation of the (3__R__)‐ and (3__S__)‐diastereomers was carried out via the 3‐phenyl‐2,3,10,10a‐tetrahydro‐5H‐imidazo[1,5‐b]isoquinolin‐

Preparation of carbon-14-labeled (3R)-7-

Preparation of carbon-14-labeled (3R)-7-hydroxy-N-(1S)-1-{[(3R,4R)-4-(3-hydroxyphenyl)-3,4-dimethyl-1-piperidinyl]methyl}-2-methylpropyl-1,2,3,4-tetrahydroisoquinolinecarboxamide (JDTic)

✍ Bertold D. Berrang; Anita H. Lewin; F. Ivy Carroll 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 French ⚖ 86 KB 👁 1 views