Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 223,630,642 papers from all fields of science
Search
Sign In
Create Free Account
Styrenes
Known as:
Styrenes [Chemical/Ingredient]
Derivatives and polymers of styrene. They are used in the manufacturing of synthetic rubber, plastics, and resins. Some of the polymers form the…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
50 relations
Narrower (45)
1,1-diphenylethylene
1-ethenyl-4-methylbenzene
2,5-diphenyl-1,4-distyrylbenzene
2,6-dichlorostyrene
Expand
In Blood
Polystyrenes
agonists
antagonists & inhibitors
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Regioselective radical aminofluorination of styrenes.
Hongwei Zhang
,
Yongcheng Song
,
Jinbo Zhao
,
Jingping Zhang
,
Qian Zhang
Angewandte Chemie
2014
Corpus ID: 12358304
The copper-catalyzed radical aminofluorination of styrenes with N-fluorobenzenesulfonimide (NFSI) is realized with high…
Expand
Review
2012
Review
2012
Transition-Metal-Free Coupling Reactions of Aryl Halides
E. Shirakawa
,
Tamio Hayashi
2012
Corpus ID: 98021842
Review: [recent transition-metal-free coupling reactions of aryl halides with arenes, alkenes, or aryl Grignard reagents in view…
Expand
Highly Cited
2011
Highly Cited
2011
Rhodium-catalyzed selective olefination of arene esters via C-H bond activation.
Sae Hume Park
,
Ji Young Kim
,
Sukbok Chang
Organic Letters
2011
Corpus ID: 10341501
A new catalytic procedure of ortho-olefination of benzoates and benzaldehydes has been developed. Ester and carboxaldehyde units…
Expand
Highly Cited
2010
Highly Cited
2010
Rh(III)-catalyzed oxidative coupling of N-aryl-2-aminopyridine with alkynes and alkenes.
Jinlei Chen
,
G. Song
,
Chengling Pan
,
Xingwei Li
Organic Letters
2010
Corpus ID: 26854994
[RhCp*Cl(2)](2) (1-2 mol %) can catalyze the oxidative coupling of N-aryl-2-aminopyridines with alkynes and arylates to give N-(2…
Expand
Highly Cited
2006
Highly Cited
2006
Kinetic studies of reactions of iron(IV)-oxo porphyrin radical cations with organic reductants.
Zhengzheng Pan
,
Rui Zhang
,
M. Newcomb
Journal of Inorganic Biochemistry
2006
Corpus ID: 24147731
Highly Cited
2002
Highly Cited
2002
Generation of substituted styrenes via Suzuki cross-coupling of aryl halides with 2,4,6-trivinylcyclotriboroxane.
F. Kerins
,
D. O’Shea
Journal of Organic Chemistry
2002
Corpus ID: 40542895
The synthesis of functionalized styrene derivatives can be readily achieved utilizing a Suzuki cross-coupling protocol between…
Expand
Highly Cited
2001
Highly Cited
2001
Asymmetric hydrosilylation of styrenes catalyzed by palladium-MOP complexes: ligand modification and mechanistic studies.
Tamio Hayashi
,
S. Hirate
,
Kenji Kitayama
,
H. Tsuji
,
A. Torii
,
Y. Uozumi
Journal of Organic Chemistry
2001
Corpus ID: 2545360
In the palladium-catalyzed asymmetric hydrosilylation of styrene (3a) with trichlorosilane, several chiral monophosphine ligands…
Expand
Highly Cited
1998
Highly Cited
1998
Controlled/"Living" Radical Polymerization of 2-(Dimethylamino)ethyl Methacrylate.
Xuan Zhang
,
J. Xia
,
K. Matyjaszewski
Macromolecules
1998
Corpus ID: 8212807
Poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) and quanternized PDMAEMA have attracted much attention in recent years as…
Expand
1994
1994
Relationship of active site topology to substrate specificity for cytochrome P450terp (CYP108).
J. Fruetel
,
R. Mackman
,
J. Peterson
,
P. Ortiz de Montellano
Journal of Biological Chemistry
1994
Corpus ID: 17955310
Highly Cited
1987
Highly Cited
1987
Synthesis of functionalized styrenes via palladium-catalyzed coupling of aryl bromides with vinyl tin reagents
D. R. Mckean
,
G. Parrinello
,
A. F. Renaldo
,
J. Stille
1987
Corpus ID: 98553327
Copulation entre le (tributylvinyl) stannane et des bromoethers, bromoaldehydes, bromocetones et des composes dibromes…
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