X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
polymer science (4) 4
analysis (3) 3
bis catalyst (3) 3
catalysis (3) 3
catalysts (3) 3
chemistry, multidisciplinary (3) 3
structure of the polymers (3) 3
1,5‐diene (2) 2
aldehydes (2) 2
allylsilane (2) 2
branched (2) 2
cycloocta‐1,5‐diene (2) 2
enantiomers (2) 2
enantioselektivität (2) 2
fluorescence (2) 2
insecticides (2) 2
iridium (2) 2
joining (2) 2
polymers (2) 2
polyphenylacetylene (2) 2
stereoselectivity (2) 2
synthesis (2) 2
transformations (2) 2
utilities (2) 2
-anatoxin-a (1) 1
-p- (1) 1
-p-[ (1) 1
1 5-diene (1) 1
1,5-diene (1) 1
1,5‐cyclooctadiene‐cucl catalysis (1) 1
1-hexene polymerization (1) 1
5-[ethynyl]-n,n-dimethylnaphthalen-1-amine (1) 1
5-ethynyl-n,n- dimethylnaphthalen-1-amine (1) 1
5-ethynyl-n,n-dimethylnaphthalen-1-amine (1) 1
5‐[ethynyl]‐n,n‐dimethylnaphthalen‐1‐amine (1) 1
5‐ethynyl‐n,n‐dimethylnaphthalen‐1‐amine (1) 1
acetylenes (1) 1
acetylenic derivatives (1) 1
alcohols (1) 1
alkaloids (1) 1
alkenylboronic acids (1) 1
alkylation (1) 1
allyl-alcohol (1) 1
allylalkohol (1) 1
allylic substitution (1) 1
allylische substitution (1) 1
alpha-allylation (1) 1
amination (1) 1
anatoxin a (1) 1
asymmetric 1,4-addition (1) 1
asymmetric-synthesis (1) 1
asymmetry (1) 1
atom economy (1) 1
bent (1) 1
benzene (1) 1
benzoyl-coa reductase (1) 1
benzoyl‐coa reductase (1) 1
biochemistry & molecular biology (1) 1
block-copolymers (1) 1
boronic acid, aryl (1) 1
boronic acids (1) 1
bound ru complex (1) 1
carbonyl compounds, α,β‐unsaturated (1) 1
chloro (1) 1
cis (1) 1
coenzyme-a (1) 1
common intermediate (1) 1
conjugate addition (1) 1
conjugated polymers (1) 1
construction (1) 1
cyclohexa-1,5-diene-1-carboxyl-coa hydratase (1) 1
cyclohexa‐1,5‐diene‐1‐carboxyl‐coa hydratase (1) 1
cyclopentadienylpalladium (1) 1
cyclopolymerisation (1) 1
cyclopolymerisations (1) 1
cyclopolymerization (1) 1
dearomatization (1) 1
degradation (1) 1
dibromoplatinum (1) 1
dichloro complex (1) 1
diene complex (1) 1
dienoyl-coa hydratase (1) 1
dienoyl‐coa hydratase (1) 1
donator-akzeptor-komplex (1) 1
efficient (1) 1
efficient heterogeneous oxidation (1) 1
enantio-selectivity (1) 1
enantioselective cyclopolymerization (1) 1
enantioselectivity (1) 1
enoyl-coa hydratase (1) 1
enoyl‐coa hydratase (1) 1
epoxide opening (1) 1
extended pi-conjugation (1) 1
extreme values (1) 1
flight mass-spectrometry (1) 1
glucosylation (1) 1
h3-allylpalladium (1) 1
h3‐allylpalladium (1) 1
hexa-1,5-diene (1) 1
hexa‐1,5‐diene (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Angewandte Chemie International Edition, ISSN 1433-7851, 09/2014, Volume 53, Issue 40, pp. 10759 - 10762
An enantioselective allyl–allylsilane cross‐coupling involving racemic branched allylic alcohols and allylsilanes is reported. An iridium‐(P,olefin)... 
enantioselectivity | iridium | 1,5‐diene | allylic substitution | allylsilane | 1 5-diene | SUBSTITUTION | ATOM ECONOMY | ALKYLATION | ALDEHYDES | CHEMISTRY, MULTIDISCIPLINARY | ALCOHOLS | AMINATION | 1,5-diene | CONSTRUCTION | REGIO | ALPHA-ALLYLATION | DEAROMATIZATION | Enantiomers | Insecticides | Analysis | Utilities | Synthesis | Asymmetry | Catalysts | Branched | Joining | Transformations | Alcohols
Journal Article
Angewandte Chemie, ISSN 0044-8249, 09/2014, Volume 126, Issue 40, pp. 10935 - 10938
An enantioselective allyl–allylsilane cross‐coupling involving racemic branched allylic alcohols and allylsilanes is reported. An iridium‐(P,olefin)... 
1,5‐Diene | Enantioselektivität | Iridium | Allylsilane | Allylische Substitution | Enantiomers | Insecticides | Analysis | Stereoselectivity | Utilities | Synthesis | Catalysts | Branched | Joining | Transformations | Catalysis
Journal Article
Helvetica Chimica Acta, ISSN 0018-019X, 01/2006, Volume 89, Issue 1, pp. 134 - 137
The synthesis of racemic anatoxin a (1a) from cycloocta‐1,5‐diene via its 1 : 1 cycloadduct with N‐chlorosulfonyl isocyanate is described. The N‐unsubstituted... 
Alkaloids | Cycloocta‐1,5‐diene | Weinreb amide | Anatoxin a | COMMON INTERMEDIATE | ASYMMETRIC-SYNTHESIS | (+)-ANATOXIN-A | (+/-)-ANATOXIN-A | (-)-ANATOXIN-A | EFFICIENT | CHEMISTRY, MULTIDISCIPLINARY | TACAMONINE
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 12/1992, Volume 30, Issue 13, pp. 2781 - 2790
Thermal degradation of poly((E,E)‐[6.2]paracyclophane‐1,5‐diene) is studied in inert and oxidative environments by using thermogravimetric analysis, pyrolysis... 
poly((E,E)‐[6.2]paracyclophane‐1,5‐diene | thermal degradation | thermal analysis | POLY((E,E)-[6.2]PARACYCLOPHANE-1,5-DIENE | POLYMER SCIENCE | BENZENE | THERMAL ANALYSIS | THERMAL DEGRADATION | BENT
Journal Article
Liebigs Annalen der Chemie, ISSN 0170-2041, 1991, Volume 1991, Issue 6, pp. 545 - 552
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.