Author:
Shaw John T.,O'Connor Mary E.,Allen Richard C.,Westler William M.,Stefanko Bruce D.
Reference11 articles.
1. J. T. Shaw, W. M. Westler and B. D. Stefanko, Chem. Commun., 1070 (1972).
2. The structure of II' could also be N-Cyano-N-(4-amino-6-methyl-2-pyrimidyl)acetamidine); either structure would give III on reaction with acetic anhydride.
3. See footnote (i) in Table I; the lack of solubility of IIb in glyme under these reaction conditions may have contributed to the lower yield of IIIb, since use of 2-methoxyethanol (in which IIb is soluble) resulted in a 37% yield of crude IIIb.
4. Synthesis of Antimalarials. VI.1 Synthesis of Certain 1,5- and 1,8-Naphthyridine Derivatives2
5. CYCLIZATION OF 2-AMINOPYRIDINE DERIVATIVES. II. THE REACTION OF SUBSTITUTED 2-AMINOPYRIDINES WITH ETHYL MALONATE1
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