Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 233,297,208 papers from all fields of science
Search
Sign In
Create Free Account
acetol
Known as:
hydroxy-2-propanone
, hydroxyacetone
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
2 relations
Broader (1)
Acetone
analogs & derivatives
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Thermal Decomposition of Electronic Cigarette Liquids
R. P. Jensen
2016
Corpus ID: 99992997
.............................................................................................................................. i…
Expand
2011
2011
Asymmetric syn-selective direct aldol reaction of protected hydroxyacetone catalyzed by primary amino acid derived bifunctional organocatalyst in the presence of water.
Akshay Kumar
,
Sarbjit Singh
,
Vikas Kumar
,
S. Chimni
Organic and biomolecular chemistry
2011
Corpus ID: 23500948
A new series of water compatible primary-tertiary diamine catalysts derived from natural primary amino acids bearing a…
Expand
2011
2011
Kinetics and mechanism of the glyoxal + HO2 reaction: conversion of HO2 to OH by carbonyls.
G. Silva
2011
Corpus ID: 196832168
The kinetics of the glyoxal + HO(2) reaction have been investigated using computational chemistry and statistical reaction rate…
Expand
2011
2011
Identification and Characterization of a Mycobacterial (2R,3R)-2,3-Butanediol Dehydrogenase
M. Takeda
,
T. Muranushi
,
+4 authors
J. Koizumi
Bioscience, biotechnology and biochemistry
2011
Corpus ID: 35824101
Bacterial strain B-009, capable of using racemic 1,2-propanediol (PD), was identified as a rapid-growing member of the genus…
Expand
2009
2009
N-primary-amine-terminal beta-turn tetrapeptides as organocatalysts for highly enantioselective aldol reaction.
Feng-Chun Wu
,
Chao‐Shan Da
,
+5 authors
Xiao Ma
Journal of Organic Chemistry
2009
Corpus ID: 45947873
Tetrapeptides, containing a terminated primary amine and conformationally restricted D-Pro-Gly or D-Pro-Aib (2-aminoisobutanoic…
Expand
2009
2009
Experimental and theoretical studies of the kinetics of the OH + hydroxyacetone reaction as a function of temperature.
M. Baasandorj
,
S. Griffith
,
S. Dusanter
,
P. Stevens
Journal of Physical Chemistry A
2009
Corpus ID: 22954137
The rate constant for the reaction of the OH radical with hydroxyacetone was measured between 2 and 5 Torr and over the…
Expand
2008
2008
Biosynthesis of isoprenoids – studies on the mechanism of 2C‐methyl‐d‐erythritol‐4‐phosphate synthase
S. Lauw
,
V. Illarionova
,
A. Bacher
,
F. Rohdich
,
W. Eisenreich
The FEBS Journal
2008
Corpus ID: 42719087
2C‐Methyl‐d‐erythritol‐4‐phosphate synthase, encoded by the ispC gene (also designated dxr), catalyzes the first committed step…
Expand
2007
2007
Products and Functional Group Distributions in Pyrolysis Oil of Chromated Copper Arsenate (CCA)-Treated Wood, as Elucidated by Gas Chromatography and a Novel 31P NMR-Based Method
Q. Fu
,
D. Argyropoulos
,
D. Tilotta
,
L. Lucia
2007
Corpus ID: 98452457
Low-temperature pyrolysis offers a feasible option for wood waste management and the recovery of a variety of useful chemicals…
Expand
2002
2002
Biosynthesis of terpenes. Preparation of (E)-1-hydroxy-2-methyl-but-2-enyl 4-diphosphate, an intermediate of the deoxyxylulose phosphate pathway.
S. Amslinger
,
Klaus Kis
,
+5 authors
W. Eisenreich
Journal of Organic Chemistry
2002
Corpus ID: 23035742
(E)-1-hydroxy-2-methyl-but-2-enyl 4-diphosphate (E-6) was synthesized in six reaction steps from hydroxyacetone (9) and…
Expand
1998
1998
Total Syntheses of the Cytotoxic Marine Natural Product, Aplysiapyranoid C1
M. Jung
,
B. Fahr
,
D. D'amico
1998
Corpus ID: 4942034
The first total syntheses of the cytotoxic marine natural product, aplysiapyranoid C, 1c, are reported. The Wittig reaction of 4…
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