High-yielding syntheses of 4(5)-substituted imidazoles via organolithium intermediates. the utility of sulphonamide n-protection and silicon-containing blocking groups-Reference-Cited by-同舟云学术

High-yielding syntheses of 4(5)-substituted imidazoles via organolithium intermediates. the utility of sulphonamide n-protection and silicon-containing blocking groups

Published:1986-01 Issue:8 Volume:42 Page:2351-2358
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Carpenter Andrew J.,Chadwick Derek J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. Regioselective α- and β-metallations of thiophene derivatives bearing the 4,4-dimethyloxazolin-2-yl group. Application of the method to syntheses of 2,3- and 2,5-disubstituted thiophene derivatives

2. High-yield syntheses of 2,3-disubstituted furans and thiophenes

3. 2,5-Dilithiation of N-protected imidazoles. Syntheses of 2,5-disubstituted derivatives of 1-methoxymethyl-, 1-triphenylmethyl-, and 1-(N,N-dimethylsulphonamido)-imidazole

4. Metallation and Metal-halogen Exchange Reactions of Imidazoles

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