1998
DOI: 10.1002/(sici)1098-1071(1998)9:3<341::aid-hc11>3.0.co;2-r
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A facile preparation of 2,6-diarylpyrazines

Abstract: 2,6‐Diarylpyrazines were prepared in good yields by a novel method of condensing methoxycarbonylhydrazine with N,N‐bis(arylcarbonylmethyl)‐p‐toluenesulfonamides, unsymmetrical derivatives of which were synthesized by a new (or different) procedure. The structures of these 2,6‐diarylpyrazines were established by spectral data and X‐ray diffraction analysis. © 1998 John Wiley & Sons, Inc. Heteroatom Chem 9:341–345, 1998

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Cited by 10 publications
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“…Pyrazines are also synthesized using α-halo ketones 16 or by the condensation reaction of diamines and epoxides. 17 Dehydrogenation of piperazines to form pyrazine derivatives was also reported using heterogeneous catalysts.…”
mentioning
confidence: 99%
“…Pyrazines are also synthesized using α-halo ketones 16 or by the condensation reaction of diamines and epoxides. 17 Dehydrogenation of piperazines to form pyrazine derivatives was also reported using heterogeneous catalysts.…”
mentioning
confidence: 99%
“…Accordingly, considerable attention has been paid to the development of efficient approaches to their synthesis 10. 11 However, secondary α‐sulfonylamino ketones 4 cannot be prepared directly from sulfamide and 2‐bromoacetophenone 12. These types of α‐amino ketones are constructed from the ring‐opening of aziridines10ad or the oxidation of allylic amines 10e.…”
Section: Methodsmentioning
confidence: 99%
“…Subsequent cyclization with hydrazine led to the formation of unsymmetrical 2,6-disubstituted pyrazines. 16 Another group developed a microwave strategy to unsymmetrical 2,6-disubstituted pyrazines through an intramolecular hydroamination sequence (Scheme 1B). 17 However, there still remained the issue of…”
mentioning
confidence: 99%