Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 37, 2007 - Issue 2
Submit an article Journal homepage
168
Views
9
CrossRef citations to date
0
Altmetric
Original Articles

Efficient Synthesis of 3,5,6‐Trisubstituted‐1,2,4‐triazines in the Brønsted Acidic Ionic Liquid, 1‐n‐Butylimidazolium Tetrafluoroborate ([Hbim]BF4)

T. M. Potewar Division of Organic Chemistry, Technology National Chemical Laboratory, Pune, India
,
R. J. Lahoti Division of Organic Chemistry, Technology National Chemical Laboratory, Pune, India
,
Thomas Daniel Division of Organic Chemistry, Technology National Chemical Laboratory, Pune, India
&
K. V. Srinivasan Division of Organic Chemistry, Technology National Chemical Laboratory, Pune, IndiaCorrespondence[email protected]
Pages 261-269 | Received 22 Jun 2006, Published online: 25 Jul 2007

Citations (9)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (2)

RiyajS. Tamboli, Rajani Giridhar, HemantM. Mande, ShaileshR. Shah & Mange Ram Yadav. (2014) Room-Temperature Ionic Liquid–DMSO Promoted and Improved One-Pot Synthesis of 5,6-Diaryl-1,2,4-triazines. Synthetic Communications 44:15, pages 2192-2204.
Read now
K. Venkatesan, SureshS. Pujari & KumarV. Srinivasan. (2008) Proline-Catalyzed Simple and Efficient Synthesis of 1,8-Dioxo-decahydroacridines in Aqueous Ethanol Medium. Synthetic Communications 39:2, pages 228-241.
Read now

Articles from other publishers (7)

Alahyar Emami-Nori, Zahra Karamshahi & Ramin Ghorbani-Vaghei. (2021) Efficient Synthesis of Multiply Substituted Triazines Using GO@N-Ligand-Cu Nano-Composite as a Novel Catalyst. Journal of Inorganic and Organometallic Polymers and Materials 31:4, pages 1801-1810.
Crossref
Ramin Ghorbani-Vaghei, Azadeh Shahriari, Zahra Salimi & Somayeh Hajinazari. (2015) Solvent-free synthesis of triazines using N-halosulfonamides. RSC Advances 5:5, pages 3665-3669.
Crossref
Rajesh G. Kalkhambkar, Sarah N. Waters & Kenneth K. Laali. (2011) Highly efficient synthesis of amides via Ritter chemistry with ionic liquids. Tetrahedron Letters 52:8, pages 867-871.
Crossref
Dmitry N. Kozhevnikov & Valery N. Kozhevnikov. 2009. 415 434 .
V. Charushin, V. Rusinov & O. Chupakhin. 2008. Comprehensive Heterocyclic Chemistry III. Comprehensive Heterocyclic Chemistry III 95 196 .
T. M. Potewar, R. J. Lahoti, Thomas Daniel & K. V. Srinivasan. (2007) Efficient Synthesis of 3,5,6‐Trisubstituted‐1,2,4‐triazines in the Broensted Acidic Ionic Liquid, 1‐n‐Butylimidazolium Tetrafluoroborate ([Hbim]BF 4 ). . ChemInform 38:26.
Crossref
Abigail Hubbard, Takao Okazaki & Kenneth K. Laali. (2007) Chlorination of Aromatics with Trichloroisocyanuric Acid (TCICA) in Brønsted-Acidic Imidazolium Ionic Liquid [BMIM(SO3H)][OTf]: an Economical, Green Protocol for the Synthesis of Chloroarenes. Australian Journal of Chemistry 60:12, pages 923.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.