Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 35, 2005 - Issue 18
Submit an article Journal homepage
148
Views
9
CrossRef citations to date
0
Altmetric
Original Articles

Pinacol Coupling Reaction of Aromatic Aldehydes Mediated by Aqueous Vanadium(II) Solution Under Ultrasound Irradiation

Shu‐Xiang Wang College of Chemistry and Environmental Science, Hebei University, Hebei Province, Baoding, China; Key Laboratory of Analytical Science and Technology, Hebei Province, Baoding, China
,
Ke Wang College of Chemistry and Environmental Science, Hebei University, Hebei Province, Baoding, China; Key Laboratory of Analytical Science and Technology, Hebei Province, Baoding, China
&
Ji‐Tai Li College of Chemistry and Environmental Science, Hebei University, Hebei Province, Baoding, China; Key Laboratory of Analytical Science and Technology, Hebei Province, Baoding, ChinaCorrespondence[email protected]
Pages 2387-2394 | Received 21 Feb 2005, Published online: 18 Aug 2006

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 (1)

Ying Xin, Zhi-He Zang & Feng-Lei Chen. (2009) Ultrasound-Promoted Synthesis of 1,5-Diarylpenta-2,4-dien-1-ones Catalyzed by Activated Barium Hydroxide. Synthetic Communications 39:22, pages 4062-4068.
Read now

Articles from other publishers (8)

Carlos M. Teixeira, Pedro Adão, M. Fernanda N.N. Carvalho, Clara S.B. Gomes & João Costa Pessoa. (2020) -Phenylalanine derived tripodal vanadium complexes as catalysts for the asymmetric reductive coupling of benzaldehyde. Inorganica Chimica Acta 510, pages 119727.
Crossref
Richard C. LarockRichard C. Larock & Cristiano Raminelli. 2018. Comprehensive Organic Transformations. Comprehensive Organic Transformations 1 69 .
Muriel Billamboz, Claire Imbs, Estelle Banaszak-Léonard & Christophe Len. (2017) Selective One-Pot Three-Step Cascade Reaction: From Aromatic Aldehydes to 2,2-Diphenylethanol Derivatives. Organic Process Research & Development 21:6, pages 835-843.
Crossref
Muriel Billamboz & Christophe Len. (2015) First Pinacol Coupling in Emulsified Water: Key Role of Surfactant and Impact of Alternative Activation Technologies. ChemSusChem 8:10, pages 1664-1675.
Crossref
Zerong Wang. 2010. Comprehensive Organic Name Reactions and Reagents. Comprehensive Organic Name Reactions and Reagents 2221 2226 .
Vivek Polshettiwar & Rajender S. Varma. 2010. Handbook of Green Chemistry. Handbook of Green Chemistry 273 290 .
Hongwei Yang, Hongsong Wang & Chengjian Zhu. (2007) Enantioselective Pinacol Coupling of Aryl Aldehydes Catalyzed by Chiral Salan−Mo(IV) Complexes. The Journal of Organic Chemistry 72:26, pages 10029-10034.
Crossref
Shu‐Xiang Wang, Ke Wang & Ji‐Tai Li. (2006) Pinacol Coupling Reaction of Aromatic Aldehydes Mediated by Aqueous Vanadium(II) Solution under Ultrasound Irradiation.. ChemInform 37:5.
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.