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  • Facile, selective, and regiocontrolled synthesis of oxazolines and oxazoles mediated by ZnI2 and FeCl3.

Facile, selective, and regiocontrolled synthesis of oxazolines and oxazoles mediated by ZnI2 and FeCl3.

Organic letters (2012-08-11)
Gopal Chandru Senadi, Wan-Ping Hu, Jia-Shing Hsiao, Jaya Kishore Vandavasi, Chung-Yu Chen, Jeh-Jeng Wang
ABSTRACT

An expedient method for a direct approach to the selective and regiocontrolled synthesis of 2-oxazolines and 2-oxazoles mediated by ZnI(2) and FeCl(3) is described. A Lewis acid promoted cyclization of acetylenic amide with various functionalities was well tolerated to give 2-oxazolines and 2-oxazoles in good to excellent yields under mild reaction conditions.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Zinc iodide, anhydrous, powder, 99.999% trace metals basis
Sigma-Aldrich
Zinc iodide, purum p.a., ≥98.0% (AT)
Sigma-Aldrich
Zinc iodide, ≥99.99% trace metals basis
Sigma-Aldrich
Zinc iodide, ≥98%