Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,258,698 papers from all fields of science
Search
Sign In
Create Free Account
3-buten-2-one
Known as:
methyl vinyl ketone
, methylvinyl ketone
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
Broader (1)
Butanones
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2015
Highly Cited
2015
ProPhenol-Catalyzed Asymmetric Additions by Spontaneously Assembled Dinuclear Main Group Metal Complexes
B. Trost
,
Mark J. Bartlett
Accounts of Chemical Research
2015
Corpus ID: 40897001
Conspectus The development of catalytic enantioselective transformations has been the focus of many research groups over the past…
Expand
Highly Cited
2011
Highly Cited
2011
Palladium-catalyzed diastereo- and enantioselective synthesis of substituted cyclopentanes through a dynamic kinetic asymmetric formal [3+2]-cycloaddition of vinyl cyclopropanes and alkylidene…
B. Trost
,
Patrick J. Morris
Angewandte Chemie
2011
Corpus ID: 570030
The development of new enantioselective methods for the formation of cyclopentane rings containing multiple stereocenters is of…
Expand
Highly Cited
2008
Highly Cited
2008
Oxidation-resistant fluorogenic probe for mercury based on alkyne oxymercuration.
Fengling Song
,
Shuji Watanabe
,
P. Floreancig
,
K. Koide
Journal of the American Chemical Society
2008
Corpus ID: 207130303
Mercury continues to be a major safety hazard to the general public. Therefore, a fluorescence method that has potential for on…
Expand
Highly Cited
2007
Highly Cited
2007
Organocatalytic sequential one-pot double cascade asymmetric synthesis of Wieland-Miescher ketone analogues from a Knoevenagel/hydrogenation/Robinson annulation sequence: scope and applications of…
Dhevalapally B. Ramachary
,
M. Kishor
Journal of Organic Chemistry
2007
Corpus ID: 497679
A practical and novel organocatalytic chemo- and enantioselective process for the cascade synthesis of highly substituted 2-alkyl…
Expand
Highly Cited
2005
Highly Cited
2005
Chiral phosphine lewis bases catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with activated olefins.
M. Shi
,
Lian Chen
,
Chao Li
Journal of the American Chemical Society
2005
Corpus ID: 36287920
In the aza-Baylis-Hillman reaction of N-sulfonated imines (N-arylmethylidene-4-methylbenzenesulfonamides and others) with methyl…
Expand
Highly Cited
2003
Highly Cited
2003
Chiral phosphine Lewis base catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone and phenyl acrylate.
M. Shi
,
Lian Chen
Chemical Communications
2003
Corpus ID: 11437031
In the aza-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone (MVK) promoted by chiral phosphine Lewis base…
Expand
Highly Cited
2003
Highly Cited
2003
Direct enantioselective Michael addition of aldehydes to vinyl ketones catalyzed by chiral amines.
P. Melchiorre
,
K. A. Jørgensen
Journal of Organic Chemistry
2003
Corpus ID: 28330552
Chiral amines such as (S)-2-[bis(3,5-dimethylphenyl)methyl]pyrrolidine and the C(2)-symmetric (2S,5S)-2,5-diphenylpyrrolidine can…
Expand
Highly Cited
2002
Highly Cited
2002
Catalytic, asymmetric Baylis-Hillman reaction of imines with methyl vinyl ketone and methyl acrylate.
M. Shi
,
Yong Xu
Angewandte Chemie
2002
Corpus ID: 35225525
Highly Cited
2000
Highly Cited
2000
A proline-catalyzed asymmetric Robinson annulation reaction
T. Bui
,
C. Barbas
2000
Corpus ID: 97869455
Highly Cited
1975
Highly Cited
1975
Reaction of Glutathione with Conjugated Carbonyls
H. Esterbauer
,
Helmward Zöllner
,
N. Scholz
Zeitschrift fur Naturforschung. Section C…
1975
Corpus ID: 27951006
Abstract 1. GSH reacts with conjugated carbonyls according to the equation: G SH+R-CH=CH-COR⇆R-CH(SG)-CH2-COR. The forward…
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