Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol

2016 ◽  
Vol 86 (3) ◽  
pp. 564-569
Author(s):  
I. S. Nizamov ◽  
D. A. Terenzhev ◽  
I. D. Nizamov ◽  
G. G. Shumatbaev ◽  
E. S. Batyeva ◽  
...  
Keyword(s):  
Trimethylsilyl Ethers

Mass spectrometry of the trimethylsilyl ethers of 2-ketohexoses

Tetrahedron ◽  
1970 ◽  
Vol 26 (19) ◽  
pp. 4527-4536 ◽  
Author(s):  
S. Karady ◽  
S.H. Pines
Keyword(s):  
Mass Spectrometry ◽  
Trimethylsilyl Ethers

Oxidative deprotection of tetrahydropyranyl and trimethylsilyl ethers in water using 1,4-dichloro-1,4-diazoniabicyclo[2,2,2]octane bis-chloride under neutral conditions

2007 ◽  
Vol 2007 (7) ◽  
pp. 377-380 ◽  
Author(s):  
Mahmood Tajbakhsh ◽  
Setareh Habibzadeh
Keyword(s):  
Environmentally Benign ◽  
Trimethylsilyl Ethers ◽  
Neutral Conditions ◽  
Efficient Reagent

A facile oxidative deprotection of trimethylsilyl and tetrahydropyranyl ethers in water using 1,4-dichloro-1,4-diazoniabicyclo[2,2,2]octane bis-chloride as a new efficient reagent under neutral conditions is described. This methodology is ecofriendly and environmentally benign since it uses water as a solvent. In all reactions DABCO was regenerated, rechlorinated and reused several times.

The Use of Nafion-H® as an Efficient Catalyst for the Direct Conversion of Primary and Secondary Trimethylsilyl Ethers to Their Corresponding Ethers under Mild and Heterogeneous Conditions.

ChemInform ◽  
2004 ◽  
Vol 35 (5) ◽  
Author(s):  
Mohammad Ali Zolfigol ◽  
Iraj Mohammadpoor-Baltork ◽  
Davood Habibi ◽  
BiBi Fatemeh Mirjalili ◽  
Abdolhamid Bamoniri
Keyword(s):  
Direct Conversion ◽  
Efficient Catalyst ◽  
Trimethylsilyl Ethers

Synthesis of β-amino-α-ferrocenyl alcohols

2005 ◽  
Vol 2005 (11) ◽  
pp. 712-715 ◽  
Author(s):  
Hai-Ying Zhao ◽  
Zhan-Xi Bian ◽  
Bao-Guo Li
Keyword(s):  
Lithium Aluminum Hydride ◽  
Aluminum Hydride ◽  
Chain Structure ◽  
Lithium Aluminum ◽  
Polymeric Chain ◽  
X Ray ◽  
H Nmr ◽  
Hydrogen Bonding Interactions ◽  
Trimethylsilyl Ethers ◽  
New Compounds

β-Amino-α-ferrocenyl alcohols [FcC(OH)(R)CH2NH2] (R = Me, Et, nPr, iPr, Ph, p-MeOC6H4, o-ClC6H4, m-ClC6H4, p-ClC6H4, Fc; Fc = C5H4FeC5H5) were prepared by the reduction of cyanohydrin trimethylsilyl ethers of acylferrocenes with lithium aluminum hydride. All new compounds were characterised by elemental analysis, IR and 1H NMR spectroscopies. The X-ray crystal structure of β-amino-α,α-diferrocenylethanol shows that it has a polymeric chain structure with hydrogen bonding interactions between the OH proton and the N of NH2.

A new preparation of trimethylsilyl ethers

1978 ◽  
Vol 19 (44) ◽  
pp. 4261-4262 ◽  
Author(s):  
Harold W. Pinnick ◽  
Bolkrishna S. Bal ◽  
Nordin H. Lajis
Keyword(s):  
Trimethylsilyl Ethers
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