130
Views
10
CrossRef citations to date
0
Altmetric
Original Articles

N,N′-Dibromo-N,N′-1,2-ethanediylbis (Benzene Sulfonamide) as a Novel N-Bromo Reagent–Catalyzed Trimethylsilylation of Alcohols and Phenol With Hexamethyldisilazane in Both Solution and Solvent-Free Conditions

, , &
Pages 537-544 | Received 06 Jun 2006, Accepted 10 Aug 2006, Published online: 30 Jan 2007

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

Read on this site (3)

Ardeshir Khazaei, Amin Rostami, Zahra Rosta & Ali Alavi. (2009) N,N′-Dibromo-N,N′–1,2-ethanediylbis(benzene sulfonamide) as an Efficient Catalyst for Acetylation and Formylation of Alcohols Under Mild Conditions. Phosphorus, Sulfur, and Silicon and the Related Elements 185:1, pages 181-186.
Read now
Hamid Reza Shaterian, Fahimeh Khorami, Razieh Doostmohammadi, Azita Amirzadeh & Majid Ghashang. (2009) A Facile and Efficient Trimethylsilylation of Hydroxyl Groups Using Silica-Supported Zinc Chloride and Alumina-Supported Sodium Hydrogensulfate as Recyclable Heterogeneous Catalysts. Phosphorus, Sulfur, and Silicon and the Related Elements 184:9, pages 2227-2237.
Read now

Articles from other publishers (7)

Masoomeh Norouzi & Arash Ghorbani-Choghamarani. (2016) Mild and highly efficient method for the oxidation of sulfides and protection of alcohols catalyzed by oxovanadium(IV) supported on modified magnetic nanoparticles as recyclable catalyst. Reaction Kinetics, Mechanisms and Catalysis 119:2, pages 537-554.
Crossref
Vida Saleh, Ardeshir Khazaei, Hamid Abizadeh & Shahnaz Saednia. (2015) Synthesis, Characterization, and Application of Poly(N,N′-dibromo-N-ethylnaphthyl-2,7-disulfonamide) as an Efficient Reagent for the Synthesis of 2-Arylbenzimidazole and 2-Aryl-1-arylmethyl-1H-1,3-benzimidazole Derivatives. Organic Chemistry International 2015, pages 1-9.
Crossref
Ardeshir Khazaei, Sadegh Rahmati, Ali Khalafi-nezhad & Shahnaz Saednia. (2012) Selectfluor™ F-TEDA-BF4 mediated thiocyanation or isothiocyanation of alcohols by in situ generation of [+SCN] under heterogeneous and neutral conditions. Journal of Fluorine Chemistry 137, pages 123-125.
Crossref
Arash GHORBANI-CHOGHAMARANI & Nasrin CHERAGHI-FATHABAD. (2010) Chemoselective and Catalytic Trimethylsilylation of Alcohols and Phenols by 1,1,1,3,3,3-Hexamethyldisilazane and Catalytic Amounts of PhMe3N+Br3−. Chinese Journal of Catalysis 31:9-10, pages 1103-1106.
Crossref
Ardeshir Khazaei, Sadegh Rahmati & Amin Rostami. (2009) Novel and Highly Effective Method for the Trimethylsilylation of Alcohols and Phenols with Hexamethyldisilazane (HMDS), Catalyzed by I 2 Generated in situ Using Fe(NO 3 ) 3 ⋅9 H 2 O/NaI under Heterogeneous and Neutral Conditions . Helvetica Chimica Acta 92:7, pages 1434-1438.
Crossref
Arash Ghorbani‐Choghamarani, Kamal Amani, Mohammad Ali Zolfigol, Maryam Hajjami & Roia Ayazi‐Nasrabadi. (2013) 1,3–Dichloro‐5,5–Dimethylhydantoin (DCH) and Trichloromelamine (TCM) as Efficient Catalysts for the Chemoselective Trimethylsilylation of Hydroxyl Group with 1,1,1,3,3,3–Hexamethyldisilazane (HMDS) Under Mild Conditions. Journal of the Chinese Chemical Society 56:2, pages 255-260.
Crossref
Arash Ghorbani‐Choghamarani, Mohammad Ali Zolfigol, Maryam Hajjami & Shila Jafari. (2013) Trimethylsilylation of Hydroxyl Group with 1,1,1,3,3,3‐Hexamethyldisilazane (HMDS) Catalyzed by Tribromomelamine (TBM). Journal of the Chinese Chemical Society 55:6, pages 1208-1213.
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:

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:

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.