ChemInform Abstract: First Functionalization by Metallation of the Benzene Moiety of Quinazolines. Diazines. Part 19.
โ Scribed by N. PLE; A. TURCK; V. CHAPOULAUD; G. QUEGUINER
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 35 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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โฆ Synopsis
First Functionalization by Metallation of the Benzene Moiety of Quinazolines. Diazines. Part 19.
-4-Substituted quinazolines are found to undergo unexpected regioselective lithiation at C-8. This offers an efficient pathway to a large number of new substituted quinazolines which cannot be easily prepared by other routes. All attempts to functionalize the 5 position are unsuccessful. An unexpected chlorine-lithium exchange is observed in the case of the quinazoline (XV). -(PLE, N.; TURCK, A.;
๐ SIMILAR VOLUMES
Diazines. Part 25. Functionalization by Metalation of the Benzene Moiety of Benzodiazines. Determination of Structures by Long-Range 1 H-15 N Correlation at Natural Abundance. -Direct lithiation of the benzene moiety of several benzodiazines with LiTMP is achieved in the presence of ortho-directing