Use of the vinyl group as an efficient protecting group for azole N- atoms: Synthesis of polyfunctionalized imidazoles and thieno[2,3-d] ⇌ [3,2-d]imidazole-Reference-Cited by-同舟云学术

Use of the vinyl group as an efficient protecting group for azole N- atoms: Synthesis of polyfunctionalized imidazoles and thieno[2,3-d] ⇌ [3,2-d]imidazole

Published:1997-06 Issue:26 Volume:38 Page:4647-4650
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Hartley David J.,Iddon Brian

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Azoles. Part II. Synthesis of imidazole-2(and -5)-carbaldehydes and derivatives of imidazo[1,2-b]isoquinoline; transmetallation of imidazol-5-yllithium compounds

2. Synthesis and Reactions of Lithiated Monocyclic Azoles Containing Two or More Hetero-Atoms Part IV: Imidazoles

3. Alkylation of 4(5)-Substituted Imidazoles

4. Synthesis and Reactions of Lithiated Monocyclic Azoles Containing Two or More Hetero-atoms. Part VI: Triazoles, Tetrazoles, Oxadiazoles, and Thiadiazoles

5. Generation and Reactions of sp2-Carbanionic Centers in the Vicinity of Heterocyclic Nitrogen Atoms

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