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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 16, 1986 - Issue 5
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Original Articles

Amidrazones 9. Convenient Syntheses of 1-Alkyl-1-Phenylhydrazines and α,β-Unsaturated Amidrazones Via Base-Promoted Reactions of 1,1-Disubstituted-3-Amino-4,5-Dihydro-1H-Pyrazolium Salts

Richard F. Smith Department of Chemistry, State University College of Arts and Science Geneseo, New York, 14454
,
Laurie A. Olson Department of Chemistry, State University College of Arts and Science Geneseo, New York, 14454
,
William J. Ryan Department of Chemistry, State University College of Arts and Science Geneseo, New York, 14454
,
Karen J. Coffman Department of Chemistry, State University College of Arts and Science Geneseo, New York, 14454
,
Julienne M. Galante Department of Chemistry, State University College of Arts and Science Geneseo, New York, 14454
,
Timothy S. Wojdan Department of Chemistry, State University College of Arts and Science Geneseo, New York, 14454
,
Patricia A. Mallardi Department of Chemistry, State University College of Arts and Science Geneseo, New York, 14454
&
Thomas P. Eckert Department of Chemistry, State University College of Arts and Science Geneseo, New York, 14454
 show all
Pages 585-596 | Published online: 19 Dec 2006

Citations (13)

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Read on this site (4)

Shigeru Nara, Takeshi Sakamoto, Etsuko Miyazawa & Yasuo Kikugawa. (2003) A Convenient Synthesis of 1-Alkyl-1-phenylhydrazines from -Aminophthalimide. Synthetic Communications 33:1, pages 87-98.
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Asensio González. (1991) A Convenient Preparation of 8-Ethyl-4,9-dihydro-3H-pyrano[3,4-b]indole-1-one, Key Intermediate of the Antiinflammatory Agent Etodolac. Synthetic Communications 21:5, pages 669-674.
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RichardF. Smith, KeithA. Brophy, George Rodriguez, LisaA. Dennis & WilliamJ. Ryan. (1990) Amidrazones 13. A Convenient Method for the Preparation of 1-Alkyl-1-methylhydrazines. Synthetic Communications 20:2, pages 183-188.
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Asensio González. (1988) Simple Preparation of N-Alkyl-N-Arylhydrazines from Diazotable N-Arylamines. Synthetic Communications 18:11, pages 1225-1229.
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Articles from other publishers (9)

Andrey V. Smolobochkin, Almir S. Gazizov, Alexander R. Burilov, Mikhail A. Pudovik & Oleg G. Sinyashin. (2019) Ring opening reactions of nitrogen heterocycles. Russian Chemical Reviews 88:11, pages 1104-1127.
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Thomas Zimmermann & Ortwin Brede. (2009) 3 H ‐indolium salts efficiently prepared from N ‐substituted anilines and α‐branched ketones by an one‐pot synthesis . Journal of Heterocyclic Chemistry 41:1, pages 103-108.
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Thomas Zimmermann. (2009) Ring transformations of heterocyclic compounds. XXI . Diastereoselective built‐up of an aroylcyclohexadiene moiety as second spiro‐connected ring at spiroindolines by pyrylium ring transformation . Journal of Heterocyclic Chemistry 39:2, pages 255-262.
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Thomas Zimmermann. (2009) A facile synthesis of 3 H ‐indolium perchlorates by one‐pot hydrazone formation/fischer indolization . Journal of Heterocyclic Chemistry 37:6, pages 1571-1574.
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. 1996. Comprehensive Heterocyclic Chemistry II. Comprehensive Heterocyclic Chemistry II 817 932 .
José Elguero. 1996. Comprehensive Heterocyclic Chemistry II. Comprehensive Heterocyclic Chemistry II 1 75 .
F. M. Macdonald & V. M. Lingard. 1993. Dictionary of Analytical Reagents. Dictionary of Analytical Reagents 643 709 .
Richard F. Smith, Brian H. Augustine, Lisa A. Dennis, William J. Ryan, Stephen C. Liptak & Brian R. Capparelli. (1989) Amidrazones. 12. Formation of 3-acylamino-4,5-dihydro-1,1-dimethyl-1 H -pyrazolium salts by acid-promoted cyclization of N 3 -acylated derivatives of acrylamide dimethylhydrazone and ( E )-cinnamamide dimethylhydrazone . Journal of Heterocyclic Chemistry 26:1, pages 141-143.
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R. F. SMITH, L. A. OLSON, W. J. RYAN, K. J. COFFMAN, J. M. GALANTE, T. S. WOJDAN, P. A. MALLARDI & T. P. ECKERT. (2016) ChemInform Abstract: Amidrazones. Part 9. Convenient Synthesis of 1‐Alkyl‐1‐phenylhydrazines and α,β‐Unsaturated Amidrazones via Base‐Promoted Reactions of 1,1‐Disubstituted‐ 3‐amino‐4,5‐dihydro‐1H‐pyrazolium Salts.. Chemischer Informationsdienst 17:37.
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