Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 29, 1999 - Issue 21
Submit an article Journal homepage
378
Views
10
CrossRef citations to date
0
Altmetric
Original Articles

Microwave Assisted, Highly Efficient Solid state N- and S-Alkylation

Harsha G. Jaisinghani University Department of Chemical Technology, University of Mumbai, Matunga, Mumbai, 400 019, India
&
Bhushan M. Khadilkar University Department of Chemical Technology, University of Mumbai, Matunga, Mumbai, 400 019, India
Pages 3693-3698 | Accepted 20 Jan 1999, Published online: 17 Sep 2007

Citations (10)

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)

AdelS. El-Azab & AlaaA.-M. Abdel-Aziz. (2012) An Efficient Synthesis of Thioesters Via TFA-Catalyzed Reaction of Carboxylic Acid and Thiols: Remarkably Facile C–S Bond Formation. Phosphorus, Sulfur, and Silicon and the Related Elements 187:9, pages 1046-1055.
Read now

Articles from other publishers (9)

Hamed S. Hayatshahi, Robert R. Luedtke, Michelle Taylor, Peng-Jen Chen, Benjamin E. Blass & Jin Liu. (2021) Factors Governing Selectivity of Dopamine Receptor Binding Compounds for D2R and D3R Subtypes. Journal of Chemical Information and Modeling 61:6, pages 2829-2843.
Crossref
Purushothaman Gopinath, Chanda Debasree, Ravindran Sasitha Vidyarini & Srinivasan Chandrasekaran. (2010) Synthesis of S-functionalized thioesters using thioaroylate ions derived from carboxylic acids and tetrathiomolybdate via acyloxyphosphonium intermediates. Tetrahedron 66:34, pages 7001-7011.
Crossref
Basudeb Basu, Susmita Paul & Ashis K. Nanda. (2010) Silica-promoted facile synthesis of thioesters and thioethers: a highly efficient, reusable and environmentally safe solid support. Green Chemistry 12:5, pages 767.
Crossref
I. V. Koval’. (2007) Reactions of thiols. Russian Journal of Organic Chemistry 43:3, pages 319-346.
Crossref
Sakthivel Vijaikumar & Kasi Pitchumani. (2004) Simple, solvent free syntheses of unsymmetrical sulfides from thiols and alkyl halides using hydrotalcite clays. Journal of Molecular Catalysis A: Chemical 217:1-2, pages 117-120.
Crossref
Michael B. Smith. 2003. Compendium of Organic Synthetic Methods. Compendium of Organic Synthetic Methods 264 309 .
Safdar Hayat, Atta-ur-Rahman, M Iqbal Choudhary, Khalid Mohammed Khan, Wilhelm Schumann & Ernst Bayer. (2001) N-Alkylation of anilines, carboxamides and several nitrogen heterocycles using CsF–Celite/alkyl halides/CH3CN combination. Tetrahedron 57:50, pages 9951-9957.
Crossref
Pelle Lidström, Jason Tierney, Bernard Wathey & Jacob Westman. (2001) Microwave assisted organic synthesis—a review. Tetrahedron 57:45, pages 9225-9283.
Crossref
Harsha G. Jaisinghani & Bhushan M. Khadilkar. (2010) ChemInform Abstract: Microwave Assisted, Highly Efficient Solid State N‐ and S‐Alkylation.. ChemInform 30:52.
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.