ChemInform Abstract: Skeletal Rearrangements of Deprotonated Organosilanes in the Gas Phase. Silicon-Oxygen Bond Formation.

ChemInform ◽  
1990 ◽  
Vol 21 (27) ◽  
Author(s):  
K. M. DOWNARD ◽  
J. H. BOWIE ◽  
R. N. HAYES
Keyword(s):  
Gas Phase ◽  
Bond Formation ◽  
Skeletal Rearrangements ◽  
Oxygen Bond ◽  
Silicon Oxygen

Skeletal Rearrangements of Deprotonated Organosilanes in the Gas Phase. Silicon-Oxygen Bond Formation

1990 ◽  
Vol 43 (3) ◽  
pp. 511 ◽  
Author(s):  
KM Downard ◽  
JH Bowie ◽  
RN Hayes
Keyword(s):  
Carboxylic Acid ◽  
Gas Phase ◽  
Collisional Activation ◽  
Bond Formation ◽  
Rearrangement Reactions ◽  
Skeletal Rearrangements ◽  
Oxygen Bond ◽  
Silicon Oxygen

Trimethylsilyl anions containing additional alkoxy, ketone or carboxylic acid funtionality undergo a variety of rearrangement reactions upon collisional activation. The most common are those which involve production of Si -O bonds, either by formation of Me3SiO- or by elimination of Me3SiOH.

Enzyme mediated silicon–oxygen bond formation; the use of Rhizopus oryzae lipase, lysozyme and phytase under mild conditions

2010 ◽  
Vol 39 (39) ◽  
pp. 9361 ◽  
Author(s):  
Vincenzo Abbate ◽  
Alan R. Bassindale ◽  
Kurt F. Brandstadt ◽  
Rachel Lawson ◽  
Peter G. Taylor
Keyword(s):  
Rhizopus Oryzae ◽  
Bond Formation ◽  
Rhizopus Oryzae Lipase ◽  
Mild Conditions ◽  
Oxygen Bond ◽  
Silicon Oxygen

Amine catalysed silicon–oxygen bond formation

2005 ◽  
Vol 8 (12) ◽  
pp. 1082-1084 ◽  
Author(s):  
Kaustavmoni Deka ◽  
Rupam Jyoti Sarma ◽  
Jubaraj B. Baruah
Keyword(s):  
Bond Formation ◽  
Oxygen Bond ◽  
Silicon Oxygen

A large scale enzyme screen in the search for new methods of silicon–oxygen bond formation

2011 ◽  
Vol 105 (2) ◽  
pp. 268-275 ◽  
Author(s):  
Vincenzo Abbate ◽  
Alan R. Bassindale ◽  
Kurt F. Brandstadt ◽  
Peter G. Taylor
Keyword(s):  
Large Scale ◽  
Bond Formation ◽  
New Methods ◽  
Oxygen Bond ◽  
Silicon Oxygen

Formation of Carbon-Oxygen Bond Mediated by Hypervalent Iodine Reagents Under Metal-free Conditions

2020 ◽  
Vol 17 ◽  
Author(s):  
Ayesha Jalil ◽  
Yaxin O Yang ◽  
Zhendong Chen ◽  
Rongxuan Jia ◽  
Tianhao Bi ◽  
...  
Keyword(s):  
Natural Products ◽  
Bond Formation ◽  
Building Blocks ◽  
Review Article ◽  
Hypervalent Iodine ◽  
Metal Free ◽  
Bioactive Natural Products ◽  
The Past ◽  
Oxygen Bond ◽  
Privileged Scaffolds

: Hypervalent iodine reagents are a class of non-metallic oxidants have been widely used in the construction of several sorts of bond formations. This surging interest in hypervalent iodine reagents is essentially due to their very useful oxidizing properties, combined with their benign environmental character and commercial availability from the past few decades ago. Furthermore, these hypervalent iodine reagents have been used in the construction of many significant building blocks and privileged scaffolds of bioactive natural products. The purpose of writing this review article is to explore all the transformations in which carbon-oxygen bond formation occurred by using hypervalent iodine reagents under metal-free conditions

ChemInform Abstract: New Access to H-Phosphonates via Metal-Catalyzed Phosphorus—Oxygen Bond Formation.

ChemInform ◽  
2008 ◽  
Vol 39 (1) ◽  
Author(s):  
Laetitia Coudray ◽  
Isabelle Abrunhosa-Thomas ◽  
Jean-Luc Montchamp
Keyword(s):  
Bond Formation ◽  
Metal Catalyzed ◽  
Oxygen Bond

Carbon-oxygen bond formation in electron-impact ions of acetylenic sulfoxides and sulfones

1970 ◽  
Vol 3 (2) ◽  
pp. 241-242 ◽  
Author(s):  
T. H. Kinstle ◽  
W. R. Oliver ◽  
L. A. Ochrymowycz
Keyword(s):  
Electron Impact ◽  
Bond Formation ◽  
Oxygen Bond
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