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ChemInform Abstract: First Functionalization by Metallation of the Benzene Moiety of Quinazolines. Diazines. Part 19.

โœ 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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โœฆ 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.;


๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: Diazines. Part 25.
โœ V. Gautheron Chapoulaud; I. Salliot; N. Ple; A. Turck; G. Queguiner ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 38 KB ๐Ÿ‘ 1 views

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