Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 233,201,862 papers from all fields of science
Search
Sign In
Create Free Account
trinitrophenol hydride denitratase activity
Known as:
2,4,6-trinitrophenol hydride denitratase activity
, TNP hydride denitratase activity
Catalysis of the reaction: trinitrophenol hydride Meisenheimer complex = 2,4-dinitrophenol + nitrite. Trinitrophenol is also known as TNP. [UM…
Expand
National Institutes of Health
Create Alert
Alert
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Stable iso-osmabenzenes from a formal [3+3] cycloaddition reaction of metal vinylidene with alkynols.
Qianyi Zhao
,
Lei Gong
,
Chunfa Xu
,
Jun Zhu
,
Xumin He
,
H. Xia
Angewandte Chemie
2011
Corpus ID: 35183673
The investigation on the synthesis and reactivity of metal vinylidene complexes has always been an active area, especially given…
Expand
2011
2011
Reactivity of TCNE or TCNQ derivatives of quinonoid zwitterions: platinum-induced HCN elimination vs oxidative-addition.
Thomas Kauf
,
P. Braunstein
Inorganic Chemistry
2011
Corpus ID: 29545951
The reaction of the functional, zwitterionic quinonoid molecule (6E)-4-(butylamino)-6-(butyliminio)-3-oxo-2-(1,1,2,2…
Expand
2010
2010
Activation of methane by zinc: gas-phase synthesis, structure, and bonding of HZnCH3.
M. Flory
,
A. Apponi
,
L. Zack
,
L. Ziurys
Journal of the American Chemical Society
2010
Corpus ID: 17847170
The methylzinc hydride molecule, HZnCH3, has been observed in the gas phase for the first time in the monomeric form using high…
Expand
2010
2010
Facile synthetic access to rhenium(II) complexes: activation of carbon-bromine bonds by single-electron transfer.
Yanfeng Jiang
,
O. Blacque
,
T. Fox
,
C. Frech
,
H. Berke
Chemistry
2010
Corpus ID: 2507250
The five-coordinated Re(I) hydride complexes [Re(Br)(H)(NO)(PR(3))(2)] (R=Cy 1 a, iPr 1 b) were reacted with benzylbromide…
Expand
2008
2008
Stereochemical nonrigidity of a chiral rhodium boryl hydride complex: a sigma-borane complex as transition state for isomerization.
Marius V. Câmpian
,
E. Clot
,
+5 authors
David Williamson
Journal of the American Chemical Society
2008
Corpus ID: 9679469
Experimental and computational studies are reported on half-sandwich rhodium complexes that undergo B-H bond activation with…
Expand
2007
2007
The reactions of dialkylgallium hydrides with tert-butylethynylbenzenes--a systematic investigation into the course of hydrogallation reactions.
W. Uhl
,
M. Claesener
,
S. Haddadpour
,
B. Jasper
,
A. Hepp
Dalton Transactions
2007
Corpus ID: 34569971
The reactions of bis- and tris(tert-butylethynyl)benzenes with dialkylgallium hydrides afforded two different types of products…
Expand
2001
2001
Synthesis of novel 2-azabicyclo[2.2.0]- and [2.1.1]hexanols.
G. Krow
,
W. S. Lester
,
+6 authors
K. Cannon
Journal of Organic Chemistry
2001
Corpus ID: 24777402
Methyl- and phenyl-substituted N-(ethoxycarbonyl)-2-azabicyclo[2.2.0]hex-5-enes 6 were reacted with NBS in wet DMSO to afford…
Expand
2001
2001
Dialkylaluminum hydrazides derived from free hydrazine N2H4. Molecular Structures of [(MeC)2AlN2H3]2 and [(MeC)2Al]4(N2H2)2.
W. Uhl
,
J. Molter
,
B. Neumüller
Inorganic Chemistry
2001
Corpus ID: 28317774
The reaction of di(tert-butyl)aluminum hydride with hydrazine N2H4 afforded the hydrazide (Me3C)2AlN2H3, 1, by the release of…
Expand
1998
1998
Demonstration of a Directly Photopatternable Spin-On-Glass Based on Hydrogen Silsesquioxane and Photobase Generators.
Harkness
,
Takeuchi
,
Tachikawa
Macromolecules
1998
Corpus ID: 43482839
A commercially available spin-on-glass material, hydrogen silsesquioxane, has been rendered photopatternable to micrometer…
Expand
1981
1981
Synthesis and biological activity of certain derivatives of oxazinomycin and related oxadiazole nucleosides.
P. C. Srivastava
,
R. K. Robins
Journal of Medicinal Chemistry
1981
Corpus ID: 40394456
Oxazinomycin was converted into 2',3',5'-tri-O-acetyloxazinomycin (2) and 2',3'-O-isopropylideneoxazinomycin (3), respectively…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE