cas 86605-93-8, 4-bromo-α-(trimethylsilyl)toluene | Articles data ｜lookchem

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86605-93-8

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Jiangsu Xinsu New Materials Co., Ltd.
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Zibo Hangyu Biotechnology Development Co., Ltd
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Articles about 86605-93-8Total 43 be found

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SYNTHESIS STRATEGY FOR GAP PROTECTING GROUP
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Paragraph 0017; 0043

(2020/08/22)

Nanoporous Na+-montmorillonite perchloric acid as an efficient and recyclable catalyst for the chemoselective protection of hydroxyl groups
10.1166/jnn.2019.15524
Mashhadinezhad, Maryam,Shirini, Farhad,Mamaghani, Manouchehr
p. 2099 - 2107
(2019/01/03)

Graphene oxide-bound electron-deficient tin(IV) porphyrin: a highly efficient and selective catalyst for trimethylsilylation of alcohols and phenols with hexamethyldisilazane
10.1002/aoc.3568
Zarrinjahan, Alireza,Moghadam, Majid,Mirkhani, Valiollah,Tangestaninejad, Shahram,Mohammadpoor-Baltork, Iraj
(2017/02/05)

Chlorozincate(II) acidic ionic liquid: Efficient and biodegradable silylation catalyst
10.1002/aoc.3790
Abbasi, Faezeh,Azizi, Najmedin,Abdoli-Senejani, Masumeh
(2017/09/30)

Room temperature silylation of alcohols catalyzed by metal organic frameworks
10.1039/c7cy00834a
Dhakshinamoorthy, Amarajothi,Santiago-Portillo, Andrea,Concepción, Patricia,Herance, José R.,Navalón, Sergio,Alvaro, Mercedes,Garcia, Hermenegildo
p. 2445 - 2449
(2017/07/24)

Introduction of PEG-SANM nanocomposite as a new and highly efficient reagent for the promotion of the silylation of alcohols and phenols and deprotection of the silyl ethers
10.1080/10426507.2015.1119141
Shirini, Farhad,Shojaei, Abdollah Fallah,Heirati, Seyedeh Zahra Dalil
p. 944 - 951
(2016/07/06)

Preparation and characterization of a RHA/TiO2 nanocomposite: Introduction of an efficient and reusable catalyst for chemoselective trimethylsilyl protection and deprotection of alcohols and phenols
10.1039/c5ra26607f
Seddighi, Mohadeseh,Shirini, Farhad,Goli-Jolodar, Omid
p. 23564 - 23570
(2016/03/12)

Preparation of nano silica supported sodium hydrogen sulfate: As an efficient catalyst for the trimethyl, triethyl and t-butyldimethyl silylations of aliphatic and aromatic alcohols in solution and under solvent-free conditions
10.1002/jccs.201300586
Abri, Abdolreza,Ranjdar, Somayeh
p. 929 - 934
(2014/10/16)

RuIII(OTf)SalophenCH2-NHSiO2-Fe: An efficient and magnetically recoverable catalyst for trimethylsilylation of alcohols and phenols with hexamethyldisilazane
10.1002/aoc.3125
Torki, Maryam,Tangestaninejad, Shahram,Mirkhani, Valiollah,Moghadam, Majid,Mohammadpoor-Baltork, Iraj
p. 304 - 309
(2014/04/03)

Rice husk: Introduction of a green, cheap and reusable catalyst for the protection of alcohols, phenols, amines and thiols
10.1016/j.crci.2013.01.018
Shirini, Farhad,Akbari-Dadamahaleh, Somayeh,Mohammad-Khah, Ali,Aliakbar, Ali-Reza
p. 164 - 170
(2014/03/21)

Rice husk ash: A new, cheap, efficient, and reusable reagent for the protection of alcohols, phenols, amines, and thiols
10.1080/10426507.2013.844142
Shirini,Akbari-Dadamahaleh, Somayeh,Mohammad-Khah, Ali
p. 577 - 586
(2014/06/09)

Gold nanoparticles-catalyzed activation of 1,2-disilanes: Hydrolysis, silyl protection of alcohols and reduction of tert-benzylic alcohols
10.1039/c2cc35116a
Gryparis, Charis,Stratakis, Manolis
supporting information
p. 10751 - 10753,3
(2020/09/02)

Preparation, characterization and use of 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient, halogen-free and reusable ionic liquid catalyst for the trimethylsilyl protection of hydroxyl groups and deprotection of the obtained trimethylsilanes
10.1016/j.molcata.2012.08.002
Shirini, Farhad,Khaligh, Nader Ghaffari,Akbari-Dadamahaleh, Somayeh
p. 15 - 23
(2013/01/14)

Cu(NO3)2 · 3 H2O as an efficient reagent for the chemoselective trimethylsilylation of primary alcohols and oxidation of trimethylsilyl ethers
10.1080/10426507.2011.614300
Shirini,Mashhadi-Nejad
experimental part
p. 376 - 381
(2012/04/04)

Nanocrystalline TiO2-HClO4 as a new, efficient and recyclable catalyst for the chemoselective trimethylsilylation of alcohols, phenols and deprotection of silyl ethers
10.1016/j.catcom.2011.11.002
Shirini, Farhad,Atghia, Seyyed Vahid,Jirdehi, Mojtaba Ghazi
p. 5 - 10
(2013/01/15)

H3PW12O40at the[bmim][FeCl4]: A green catalytic system for alkoxymethylation of alcohols and their one-pot interconversion to acetates and TMS-ethers
10.1007/BF03249085
Mohammadpoor-Baltork,Moghadam,Tangestaninejad,Mirkhani,Khosropour,Mirjafari
experimental part
p. 513 - 524
(2012/06/16)

[InCl4]: An efficient catalyst-medium for alkoxymethylation of alcohols and their interconversion to acetates and TMS-ethers
10.1016/j.crci.2010.08.006
Mohammadpoor-Baltork, Iraj,Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah,Khosropour, Ahmad Reza,Mirjafari, Arsalan
experimental part
p. 568 - 579
(2012/05/05)

Preparation, characterization and use of 3-methyl-1-sulfonic acid imidazolium hydrogen sulfate as an eco-benign, efficient and reusable ionic liquid catalyst for the chemoselective trimethylsilyl protection of hydroxyl groups
10.1016/j.molcata.2011.08.021
Khaligh, Nader Ghaffari
experimental part
p. 63 - 70
(2011/12/02)

Succinimide-N-sulfonic acid: A mild, efficient, and reusable catalyst for the chemoselective trimethylsilylation of alcohols and phenols
10.1080/10426507.2011.602377
Shirini,Khaligh, Nader Ghaffari
experimental part
p. 2156 - 2165
(2012/04/10)

Nanocrystalline TiO2 as an efficient and reusable catalyst for the chemoselective trimethylsilylation of primary and secondary alcohols and phenols
10.1016/j.cclet.2011.05.002
Shirini, Farhad,Khoshdel, Meysam Alipour,Abedini, Masoumeh,Atghia, Seyyed Vahid
experimental part
p. 1211 - 1214
(2012/01/04)

Polyvinylpolypyrrolidoniume tribromide as new and metal-free catalyst for the formylation and trimethylsilylation of hydroxyl group
10.1016/j.cclet.2011.05.020
Ghorbani-Choghamarani, Arash,Goudarziafshar, Hamid,Zamani, Parisa
scheme or table
p. 1207 - 1210
(2012/01/05)

Protection of hydroxyl groups as a trimethylsilyl ether by 1,1,1,3,3,3-hexamethyldisilazane promoted by aspartic acid as an efficient organocatalyst
10.1016/S1872-2067(10)60210-0
Ghorbani-Choghamarani, Arash,Norouzi, Masoomeh
experimental part
p. 595 - 598
(2012/01/06)

Microwave-assisted rapid and efficient deprotection and direct esterification and silylation of MOM and EOM ethers catalyzed by [Hmim][HSO 4] as a Bronsted acidic ionic liquid
10.1007/s00706-010-0373-6
Mohammadpoor-Baltork, Iraj,Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah,Khosropour, Ahmad Reza,Mirjafari, Arsalan
experimental part
p. 1083 - 1088
(2012/06/18)

Silica-bonded S-sulfonic acid as a recyclable catalyst for the silylation of hydroxyl groups with hexamethyldisilazane (HMDS)
10.1139/V09-162
Niknam, Khodabakhsh,Saberi, Dariush,Molaee, Hajar,Zolfigol, Mohammad Ali
experimental part
p. 164 - 171
(2010/04/04)

Protection of hydroxy groups as trimethylsilyl ethers using 1,1,1,3,3,3-hexamethyldisilazane (HMDS) catalyzed BY poly(4-VINYLPYRIDINIUM TRIBROMIDE)
10.1135/cccc2009560
Ghorbani-Choghamarani, Arash,Zolfigol, Mohammad Ali,Hajjami, Maryam,Darvishi, Khorshid,Gholamnia, Laleh
experimental part
p. 607 - 615
(2011/08/05)

Nafion SAC-13: heterogeneous and reusable catalyst for the activation of HMDS for efficient and selective O-silylation reactions under solvent-free condition
10.1016/j.tet.2009.04.025
Rajagopal, Gurusamy,Lee, Hanbin,Kim, Sung Soo
experimental part
p. 4735 - 4741
(2009/10/09)

Mild and efficient silylation of alcohols and phenols with HMDS using Bi(OTf)3 under solvent-free condition
10.1016/j.jorganchem.2009.04.001
Kadam, Santosh T.,Kim, Sung Soo
experimental part
p. 2562 - 2566
(2009/12/24)

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
10.1002/jccs.200900037
Ghorbani-Choghamarani, Arash,Amani, Kamal,Zolfigol, Mohammad Ali,Hajjami, Maryam,Ayazi-Nasrabadi, Roia
experimental part
p. 255 - 260
(2009/12/06)

Chemoselective trimethylsilylation of alcohols catalyzed by saccharin sulfonic acid
10.1007/s00706-008-0004-7
Shirini, Farhad,Zolfigol, Mohammad Ali,Abedini, Masoumeh
experimental part
p. 61 - 64
(2010/03/26)

Preparation of silica supported tin chloride: As a recyclable catalyst for the silylation of hydroxyl groups with HMDS
10.1002/jccs.200900181
Niknam, Khodabakhsh,Zolfigol, Mohammad Ali,Saberi, Dariush,Molaee, Hajar
experimental part
p. 1257 - 1264
(2010/08/19)

Trimethylsilylation of hydroxyl group with 1,1,1,3,3,3-hexamethyldisilazane (HMDS) catalyzed by tribromomelamine (TBM)
10.1002/jccs.200800180
Ghorbani-Choghamarani, Arash,Zolfigol, Mohammad Ali,Hajjami, Maryam,Jafari, Shila
experimental part
p. 1208 - 1213
(2010/01/07)

Rapid and highly efficient trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) catalyzed by reusable zirconyl triflate, [ZrO(OTf)2]
10.1016/j.jorganchem.2008.03.009
Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah,Mohammadpoor-Baltork, Iraj,Chahardahcheric, Shahin,Tavakoli, Ziba
p. 2041 - 2046
(2008/09/19)

Convenient trimethylsilylation of hydroxy groups with hexamethyldisilazane under solvent-free conditions
10.1080/00304940809458091
Rostami, Amin,Khazaei, Ardeshir,Mahboubifa, Marjan,Rahmati, Sadegh
p. 303 - 306
(2008/12/20)

Vanadium hydrogen sulfate (I): Chemoselective trimethylsilylation of alcohols and deprotection of trimethylsilyl ethers
10.1002/jccs.200800140
Shirini, Farhad,Zolfigol, Mohammad Ali,Abedini, Masoumeh,Sakhaei, Ali Reza
experimental part
p. 943 - 946
(2009/12/24)

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
10.1080/10426500601013232
Khazaei, Ardeshir,Rostami, Amin,Rahmati, Sadegh,Mahboubifar, Marjan
p. 537 - 544
(2007/10/03)

Efficient trimethylsilylation of alcohols and phenols with HMDS in the presence of a catalytic amount of 1,3-dibromo-5,5-dimethylhydantoin (DBDMH) as a safe and cheap industrial chemical
10.1002/jccs.200700068
Khazaei, Ardeshir,Rostami, Amin,Mahboubifar, Marjan
p. 483 - 487
(2008/02/11)

N-Bromosuccinimide (NBS) - Selective and effective catalyst for trimethylsilylation of alcohols and phenols using hexamethyldisilazane and their regeneration under mild and neutral reaction conditions
10.1139/V07-029
Khazaei, Ardeshir,Rostami, Amin,Raiatzadeh, Ayeh,Mahboubifar, Marjan
p. 336 - 340
(2008/03/14)

A novel and highly efficient method for the direct conversion of aryl aldehyde bisulfite adducts to their aryl trimethylsilyl ethers in a one-pot manner catalyzed by montmorillonite K-10
10.1080/104265090969009
Khodaei, Mohammad M.,Khosropour, Ahmad R.,Abbasi, Jamshide
p. 93 - 97
(2007/10/03)

Efficient and convenient procedure for protection of hydroxyl groups to the THP, THF and TMS ethers and oxidation of these ethers to their aldehydes or ketones in [BPy]FeCl4 as a low cost room temperature ionic liquid
10.1515/znb-2006-0313
Khosropour, Ahmad R.,Khodaei, Mohammad M.,Ghaderi, Sattar
p. 326 - 330
(2007/10/03)

Zinc mediated reactions in organic synthesis: Efficient synthesis of silyl ethers under mild conditions
10.1002/jccs.200500019
Bandgar, Babasaheb Pandurang,Chavare, Satish Navnath,Pandit, Shivaji Sandu
p. 125 - 128
(2007/10/03)

Sulfuric acid supported on silica gel: An efficient catalyst for silylation of hydroxyl groups with HMDS and their convenient deprotection under non-aqueous condition
Lakouraj,Akbari
p. 1165 - 1167
(2007/10/03)

Reaction of carbonyl compounds with trialkylsilyl phenylselenide and tributylstannyl hydride under radical conditions
10.1021/jo025681q
Nishiyama, Yutaka,Kajimoto, Hiroyuki,Kotani, Kazuya,Nishida, Takuma,Sonoda, Noboru
p. 5696 - 5700
(2007/10/03)

Non-cluster type bismuth compounds
-
(2008/06/13)

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Chemical Properties

Melting Point: 26-29oC(lit.)
Flash Point:110oC
Density: 1.190 g/mL at 20oC(lit.)
Refractive Index: n20/D 1.531
PSA: 9.23000
LogP: 3.80060

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