Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 227,741,320 papers from all fields of science
Search
Sign In
Create Free Account
Ketones:SCnc:Pt:Bld:Qn
Known as:
??:??????:???:??:???
, Ketoonid:SCnc:Pt:B:Qn
, Ketones Sg-sCnc
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
5 relations
Blood
Chemical procedure
Ketones
SCnc
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Phosphine-catalyzed asymmetric [4+1] annulation of activated α,β-unsaturated ketones with Morita-Baylis-Hillman carbonates: enantioselective synthesis of spirooxindoles containing two adjacent…
Fang-Le Hu
,
Yin Wei
,
M. Shi
Chemical Communications
2014
Corpus ID: 205886222
The asymmetric [4+1] annulation of activated α,β-unsaturated ketones with MBH carbonates catalyzed by bifunctional thiourea…
Expand
Review
2009
Review
2009
Recent development and improvement for boron hydride-based catalytic asymmetric reduction of unsymmetrical ketones.
B. Cho
Chemical Society Reviews
2009
Corpus ID: 13349813
Catalytic asymmetric reduction of prochiral ketones with hydrides such as boranes and borohydrides is one of the simplest and the…
Expand
Highly Cited
2008
Highly Cited
2008
Combining the concepts: dual catalysis with carbophilic Lewis acids.
Alexander Duschek
,
S. Kirsch
Angewandte Chemie
2008
Corpus ID: 5048512
Highly Cited
2007
Highly Cited
2007
Gold-catalyzed intramolecular carbocyclization of alkynyl ketones leading to highly substituted cyclic enones.
T. Jin
,
Yoshinori Yamamoto
Organic Letters
2007
Corpus ID: 35400009
The reaction of the internal alkynyl ketones 1 (n=1) under the combined catalyst, AuCl3 and AgSbF6, gave the enones 2 in good to…
Expand
Highly Cited
2005
Highly Cited
2005
Catalytic asymmetric addition of alkylzinc and functionalized alkylzinc reagents to ketones.
S. Jeon
,
Hongmei Li
,
Celina García
,
Lynne K. LaRochelle
,
P. Walsh
Journal of Organic Chemistry
2005
Corpus ID: 30898839
We describe our full report of the catalytic asymmetric addition of simple and functionalized dialkylzinc reagents to a broad…
Expand
Highly Cited
2003
Highly Cited
2003
2,3,4- or 2,3,5-trisubstituted furans: catalyst-controlled highly regioselective ring-opening cycloisomerization reaction of cyclopropenyl ketones.
Shengming Ma
,
Junliang Zhang
Journal of the American Chemical Society
2003
Corpus ID: 7473388
2,3,4- or 2,3,5-trisubstituted furans were highly regioselectively formed from the cycloisomerization reaction of the same…
Expand
Highly Cited
2003
Highly Cited
2003
1,2-Migration of the thio group in allenyl sulfides: efficient synthesis of 3-thio-substituted furans and pyrroles.
Joseph T. Kim
,
A. Kel'in
,
V. Gevorgyan
Angewandte Chemie
2003
Corpus ID: 10993540
The 1,2-migration of the thio group is an important chemical transformation that is extensively used in carbohydrate chemistry…
Expand
Highly Cited
2002
Highly Cited
2002
Application of a new family of P,N ligands to the highly enantioselective hydrosilylation of aryl alkyl and dialkyl ketones.
Beata Tao
,
G. C. Fu
Angewandte Chemie
2002
Corpus ID: 28086625
Highly Cited
1999
Highly Cited
1999
Liquid Chromatography Analysis of Carbonyl (2,4-Dinitrophenyl)hydrazones with Detection by Diode Array Ultraviolet Spectroscopy and by Atmospheric Pressure Negative Chemical Ionization Mass…
E. Grosjean
,
P. G. Green
,
D. Grosjean
Analytical Chemistry
1999
Corpus ID: 27955338
The (2,4-dinitrophenyl)hydrazones of carbonyls are separated by liquid chromatography and detected by ultraviolet spectroscopy…
Expand
Highly Cited
1998
Highly Cited
1998
Direct Preparation of Trifluoromethyl Ketones from Carboxylic Esters: Trifluoromethylation with (Trifluoromethyl)trimethylsilane.
J. Wiedemann
,
Thomas Heiner
,
G. Mloston
,
G. Prakash
,
G. Olah
Angewandte Chemie
1998
Corpus ID: 14020705
Previously difficult to prepare, aliphatic and alicyclic trifluoromethylketones (e.g. 1 and 2), which are of pharmacalogic…
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