The preparation and some reactions of 2-(arylsulfonyl)vinamidinium salts
摘要:
The preparation of novel 2-(arylsulfonyl)vinamidinium salts is described. The reactions of these materials with amidines, hydrazine, hydroxylamine, sodium borohydride, and Grignard reagents are presented along with an evaluation of their chemical behavior as compared to the 2-arylvinamidinium salts.
A new route to 1,5-disubstituted 4-arylsulfonylpyrazoles by lithiation of 1-methyl-4-arylsulfonylpyrazoles
作者:Michael G. Hoffmann
DOI:10.1016/0040-4020(95)00540-o
日期:1995.8
The arylsulfonylvinamidinium salts 1 reacted with hydrazine in refluxing ethanol to give rise to 4-arylsulfonylpyrazoles 2 in reasonable yield. Regioselective lithiation of N-methylpyrazoles 3 with LDA followed by treatment with various electrophiles afforded the corresponding 1,5-disubstituted 4-arylsulfonylpyrazoles 5 in good yield.
Efficient One-Pot Synthesis of Substituted Pyrido[2,3-d]pyrimidines from Vinamidinium and Chloropropeniminium Salts
作者:Mohamed Adnen Hadj Ayed、Thouraya Gmiza、Jamel Eddine Khiari、Béchir Ben Hassine
DOI:10.1080/00397911.2010.545163
日期:2012.6.15
A novel and efficient one-pot preparation of 6-substituted pyrido-[2,3-d]pyrimidines by cyclocondensation of 6-amino-1,3-dimethyluracil with symmetrical vinamidinium salts under basic conditions has been developed. Regioselectivity was observed with an unsymmetrical chloropropeniminium salt.
GUPTON, JOHN T.;RIESINGER, STEVE W.;SHAH, AJIT S.;GALL, JOHN E.;BEVIRT, K+, J. ORG. CHEM., 56,(1991) N, C. 976-980
作者:GUPTON, JOHN T.、RIESINGER, STEVE W.、SHAH, AJIT S.、GALL, JOHN E.、BEVIRT, K+
DOI:——
日期:——
The preparation and some reactions of 2-(arylsulfonyl)vinamidinium salts
作者:John T. Gupton、Steve W. Riesinger、Ajit S. Shah、John E. Gall、Kathy M. Bevirt
DOI:10.1021/jo00003a015
日期:1991.2
The preparation of novel 2-(arylsulfonyl)vinamidinium salts is described. The reactions of these materials with amidines, hydrazine, hydroxylamine, sodium borohydride, and Grignard reagents are presented along with an evaluation of their chemical behavior as compared to the 2-arylvinamidinium salts.