Synthesis of pinacol esters of 1-alkyl-1H-pyrazol-5-yl- and 1-alkyl-1H-pyrazol-4-ylboronic acids
โ Scribed by Alexandre V. Ivachtchenko; Dmitry V. Kravchenko; Valentina I. Zheludeva; Dmitry G. Pershin
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2004
- Tongue
- English
- Weight
- 128 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0022-152X
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โฆ Synopsis
Abstract
Starting from 1__H__โpyrazol, a wide number of 1โalkylโ1__H__โpyrazolโ4โyl and 1โalkylโ1__H__โpyrazolโ5โylboronic acids and their pinacol esters were synthesized and characterized. The key step in the described methodology is the regioselective lithiation of the pyrazole ring. The synthesized pinacolates are stable under prolonged storage and can be used as convenient reagents in organic synthesis.
๐ SIMILAR VOLUMES
## Abstract A compilation of ^13^C NMR chemical shifts for 13 pairs of 3โ and 5โcyanoโsubstituted pyrazole regioisomers is reported. All of the ring carbon and cyano carbon ^13^C chemical shifts show a regular, predictable correlation with the particular isomer, whether 3โcyano or 5โcyano. These sh
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v
The facile and convenient access by a conventional procedure in ethanol as solvent to a new series of succinyl-spaced pyrazoles including 1,4-bis[5-(trichloromethyl)-5-hydroxy-4,5-dihydro-1H-pyrazol-1yl]butane-1,4-diones (64-82%) and the respective dehydrated derivatives as 1,4-bis[5-(trichloromethy