Advanced search
Publication Cover
Phosphorus, Sulfur, and Silicon and the Related Elements Volume 185, 2010 - Issue 8
Submit an article Journal homepage
258
Views
8
CrossRef citations to date
0
Altmetric
Original Articles

A Simple and Highly Efficient One-Pot Procedure for the Synthesis of Amides via Beckmann Rearrangements Using 1-Tosylimidazole (TsIm)

Mohammad Navid Soltani Rad Department of Chemistry, Faculty of Basic Sciences, Shiraz University of Technology, Shiraz, Iran
,
Ali Khalafi-Nezhad Department of Chemistry, College of Sciences, Shiraz University, Shiraz, Iran
,
Somayeh Behrouz Department of Chemistry, College of Sciences, Shiraz University, Shiraz, Iran
,
Zohreh Amini Department of Chemistry, Faculty of Basic Sciences, Shiraz University of Technology, Shiraz, Iran
&
Marzieh Behrouz Department of Chemistry, College of Sciences, Shiraz University, Shiraz, Iran
Pages 1658-1671 | Received 16 May 2009, Accepted 10 Jul 2009, Published online: 02 Aug 2010

Citations (8)

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)

Mohammad Navid Soltani Rad, Somayeh Behrouz & Abdo-Reza Nekoei. (2014) Highly Efficient One-Pot Synthesis of N-Alkyl Sulfonamides from Alcohols Using N-(p-Toluenesulfonyl) Imidazole (Tsim). Phosphorus, Sulfur, and Silicon and the Related Elements 189:4, pages 465-476.
Read now

Articles from other publishers (7)

Rita Mocci, Evelina Colacino, Lidia De Luca, Claudia Fattuoni, Andrea Porcheddu & Francesco Delogu. (2021) The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond”. ACS Sustainable Chemistry & Engineering 9:5, pages 2100-2114.
Crossref
Kamalpreet Kaur & Suman Srivastava. (2020) Beckmann rearrangement catalysis: a review of recent advances. New Journal of Chemistry 44:43, pages 18530-18572.
Crossref
Mohammad Navid Soltani Rad. (2016) A Simple, One-Pot and Phosphine-Free Procedure for Thiocyanation of Alcohols Using N-(p-toluenesulfonyl) Imidazole (TsIm). Journal of Chemical Research 40:10, pages 583-587.
Crossref
V. Yu. Kuksenok, V. V. Shtrykova, V. D. Filimonov & S. P. Sidel’nikova. (2016) Efficient one-stage procedure of Beckmann ketones rearrangement in the presence of hydroxylamine. Russian Journal of Organic Chemistry 52:2, pages 196-199.
Crossref
Fen Xu, Chunxiang Wang, Haolong Wang, Xincheng Li & Boshun Wan. (2015) Eco-friendly synthesis of pyridines via rhodium-catalyzed cyclization of diynes with oximes. Green Chemistry 17:2, pages 799-803.
Crossref
S. Chandrasekhar. 2014. Comprehensive Organic Synthesis II. Comprehensive Organic Synthesis II 770 800 .
Soon Shin, Hyuk Yoon, Seunghyun Ahn, Dong-Wook Kim, Dong-Ho Bae, Dongsoo Koh, Young Lee & Yoongho Lim. (2013) Structural Properties of Polyphenols Causing Cell Cycle Arrest at G1 Phase in HCT116 Human Colorectal Cancer Cell Lines. International Journal of Molecular Sciences 14:8, pages 16970-16985.
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.