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Who Evaluation |
Evaluation year: 2002 |
InChI:InChI=1/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3
Vanadium silicate molecular sieves can c...
A copper(I) 3,5-diphenyltriazolate metal...
Upgrading of ethanol to n-butanol throug...
This article describes new selectivities...
Reaction of (alkoxymethyl)oxiranes with ...
The structure and performance of TiO2-su...
EuCl3 dissolved in a mixture of propanoi...
In the presence of a small amount of LiB...
Taming the beast: Unprecedented selectiv...
The addition of Re to Ni on TiO2 yields ...
The combined experimental/DFT computatio...
A new method for the synthesis of dialky...
Catalytic conversion of ethanol to butan...
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Steroidal galactoside 1 and aryl esters ...
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The reactivity of active oxygen species ...
In this study, a greener and stable surf...
The straightforward reductive opening of...
In the presence of a catalytic ammount o...
Regioselectivity of hexane hydroxylation...
The reactions of alkenes with the dimeth...
Photochemical oxidation of hydrocarbons ...
Tris[bis(trimethylsilyl)amide] has been ...
Hydrogenation of the dearomatized PNN li...
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Flavor properties are important factors ...
An amide-derived N,N,N-Ru(ii) complex ca...
The osmium hydride complexes OsH2(CO)[NH...
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We previously demonstrated that Milstein...
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A putative haloalkane dehalogenase has b...
Direct conversion of tetrahydrofurfuryl ...
Palladium nanoparticles of 3.2?±?0.9?nm ...
N-Methylpyrrolidine-zinc borohydride is ...
Efficient methodologies for converting b...
In the study at hand we present a design...
Acylation of secondary alcohols using no...
A series of manganese and iron porphyrin...
A series of supported Ir-Re catalysts ha...
The upgrading of ethanol to n-butanol vi...
The reductive opening of epoxides repres...
The hydrogenation of esters catalyzed by...
We report a new chemoenzymatic cascade s...
Petroleum hydrocarbons are our major ene...
4-chlorobenzenesulfonic acid n-hexylester
4-chlorobenzenesulfinic acid
hexan-1-ol
Conditions | Yield |
---|---|
With
lithium amalgam;
In
1,4-dioxane; isopropyl alcohol;
at 23 ℃;
for 2h;
|
95% 91% |
C36H60O30*C6H14O
alpha cyclodextrin
hexan-1-ol
Conditions | Yield |
---|---|
In
water;
at 25 ℃;
Equilibrium constant;
|
ethanol
2-hexene
(2E,4E)-ethyl hexa-2,4-dienoate
oxirane
2-hexyloxyethanol
3-oxo-butyric acid-n-hexyl ester
dihexyl fumarate
hexyl nicotinate
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