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coordinated tin triflate (16) 16
silyl enol ethers (14) 14
chemistry, multidisciplinary (10) 10
chemistry, organic (6) 6
aldehydes (5) 5
asymmetric aldol reaction (5) 5
aldol reaction (4) 4
chemistry (4) 4
chemistry, inorganic & nuclear (4) 4
catalysis (3) 3
highly enantioselective synthesis (3) 3
lewis acid (3) 3
lewis-acid (3) 3
acetals (2) 2
building-blocks (2) 2
carbonyl-compounds (2) 2
catalysts (2) 2
chemical synthesis (2) 2
chiral lewis-acids (2) 2
chiral promoter (2) 2
convenient method (2) 2
cross-coupling reactions (2) 2
diels-alder reactions (2) 2
enantioselective mukaiyama-aldol (2) 2
enantioselective synthesis (2) 2
ketene acetals (2) 2
methyl-beta-hydroxy (2) 2
organic-synthesis (2) 2
oxidation (2) 2
phosphorus (2) 2
racemic secondary alcohols (2) 2
research (2) 2
syn-alpha (2) 2
synthetic methods (2) 2
trimethylsilyl chloride (2) 2
-menthyltin (1) 1
119 (1) 1
4-o-benzyl-2,3-o-isopropylidene-l-threose (1) 1
acetophenone (1) 1
alcohol acetylation catalysts (1) 1
alcohols (1) 1
alcohols - chemistry (1) 1
aldehydes - chemistry (1) 1
aldol-type reaction (1) 1
alpha-deprotonation-rearrangement (1) 1
alpha-ketophosphonates (1) 1
amino sugars (1) 1
amino-6-deoxyaldohexose (1) 1
amino-acid-derivatives (1) 1
anion trapping reactions (1) 1
anionic-polymerization (1) 1
aqueous-media (1) 1
aryl-aryl exchange (1) 1
asymmetric allylation (1) 1
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asymmetric polymerization (1) 1
baylis-hillman reaction (1) 1
benzaldehyde (1) 1
beta-diketiminato ligands (1) 1
beta-hydroxy-ketones (1) 1
bimetallic organotins (1) 1
bimetals (1) 1
biochemistry & molecular biology (1) 1
biological activity (1) 1
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biologischer prozess (1) 1
bis copper (1) 1
bisoxazolines (1) 1
bond cleavage (1) 1
bond-forming reactions (1) 1
borane complex (1) 1
butyl acrylate (1) 1
c bond formation (1) 1
c-2-symmetrical copper complexes (1) 1
c-p activation (1) 1
c-symmetric copper complexes (1) 1
cage compounds (1) 1
carbenium ion heavy analogs ‐ si‐, ge‐, sn‐ and pb‐centered cations (1) 1
carbon (1) 1
carbon multiple bonds (1) 1
carbon-phosphorus bond (1) 1
carbonyl-ene reactions (1) 1
catalyst system (1) 1
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catalytic asymmetric acylation (1) 1
catalytic asymmetric aldol (1) 1
catalytic asymmetric-synthesis (1) 1
catalyzed hydrostannylation (1) 1
cation nmr chemical shift calculation (1) 1
cations (1) 1
cations ‐ free or coordinated (1) 1
cations ‐ reactions and synthetic applications (1) 1
chalcogenide bridging (1) 1
chalcogenides (1) 1
chalcogeno carboxylic acid ester (1) 1
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Angewandte Chemie - International Edition, ISSN 1433-7851, 08/2013, Volume 52, Issue 35, pp. 9109 - 9118
A directed cross-aldol reaction of silyl enol ethers with carbonyl compounds, such as aldehydes and ketones, promoted by a Lewis acid, a reaction which is now... 
aldol reaction | silyl enol ether | stereoselectivity | history of science | synthetic methods | STANNOUS TRIFLATE | ORGANIC-SYNTHESIS | LEWIS-ACID | CONVENIENT METHOD | CARBONYL-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | TITANIUM TETRACHLORIDE | SILYL ENOL ETHERS | KETENE ACETALS | CATALYTIC ASYMMETRIC ALDOL | COORDINATED TIN(II) TRIFLATE | Aldehydes
Journal Article
Chemical Reviews, ISSN 0009-2665, 01/2008, Volume 108, Issue 1, pp. 140 - 205
Journal Article
Angewandte Chemie - International Edition, ISSN 1433-7851, 10/2004, Volume 43, Issue 42, pp. 5590 - 5614
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 1991, Volume 113, Issue 11, pp. 4247 - 4252
In the presence of a chiral promoter consisting of tin(II) triflate, a chiral diamine, and tributyltin fluoride, the silyl enol ether of S-ethyl ethanethioate... 
TRIMETHYLSILYL CHLORIDE | MICHAEL REACTION | METHYL-BETA-HYDROXY | SECONDARY PROPARGYLIC ETHERS | ENANTIOSELECTIVE SYNTHESIS | C BOND FORMATION | CONVENIENT METHOD | CHEMISTRY | CARBONYL-COMPOUNDS | CATALYST SYSTEM | COORDINATED TIN(II) TRIFLATE
Journal Article
QUIMICA NOVA, ISSN 0100-4042, 07/2003, Volume 26, Issue 4, pp. 531 - 541
Journal Article
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, ISSN 0009-2673, 06/1994, Volume 67, Issue 6, pp. 1708 - 1716
syn- and anti-1,2-Diol units were prepared by using asymmetric aldol reactions of the silyl enol ethers derived from alpha-alkoxythioacetic S-esters with... 
COMPLEX | CHIRAL PROMOTER | LEWIS ACID | SILYL ENOL ETHERS | SYN-ALPHA | OLEFINS | ALDEHYDES | ACETALS | THIOESTERS | CHEMISTRY, MULTIDISCIPLINARY | COORDINATED TIN(II) TRIFLATE
Journal Article
Chemistry Letters, ISSN 0366-7022, 5/1991, Volume 20, Issue 5, pp. 831 - 834
The stereochemistry in the aldol reaction of a silyl enol ether with chiral aldehydes is almost completely controlled by the chiral catalyst regardless of the... 
ACETALS | PROMOTER | CHEMISTRY, MULTIDISCIPLINARY | SILYL ENOL ETHERS | COORDINATED TIN(II) TRIFLATE
Journal Article
JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, ISSN 0037-9980, 07/1999, Volume 57, Issue 7, pp. 598 - 607
Journal Article
POLYMER JOURNAL, ISSN 0032-3896, 2000, Volume 32, Issue 9, pp. 722 - 728
Asymmetric group transfer polymerization (AGTP) of N-cyclohexylmaleimide (CHMI) was carried out using ketene silyl acetal as initiator in the presence of Lewis... 
Lewis acid | asymmetric polymerization | POLYMER SCIENCE | chiral ligand | ANIONIC-POLYMERIZATION | BUTYL ACRYLATE | ALDEHYDES | N-cyclohexylmaleimide | optically active polymer | CROTONATE | ALDOL REACTION | SILYL ENOL ETHERS | BISOXAZOLINES | SUBSTITUTED MALEIMIDES | CATALYSTS | group transfer polymerization | COORDINATED TIN(II) TRIFLATE
Journal Article
Chemistry Letters, ISSN 0366-7022, 6/1991, Volume 20, Issue 6, pp. 989 - 992
In the presence of a catalytic amount of chiral diamine-coordinated tin(II) triflate, acetylenic aldehydes enantioselectively react with silyl enol ethers of... 
ALDEHYDES | CHEMISTRY, MULTIDISCIPLINARY | SILYL ENOL ETHERS | COORDINATED TIN(II) TRIFLATE
Journal Article
Journal of the Chemical Society - Perkin Transactions 1, ISSN 0300-922X, 02/1998, Issue 4, pp. 709 - 715
Cyclopentadiene undergoes Diels-Alder reactions with methyl (E)- and (Z)-3-(triphenylstannyl)acrylates 5 and 6 to give the endo-cycloadduct 9, and a mixture of... 
HIGHLY ENANTIOSELECTIVE SYNTHESIS | ASYMMETRIC ALDOL REACTION | GAMMA-STANNYL ALCOHOLS | CATALYZED HYDROSTANNYLATION | LEWIS ACID | (-)-MENTHYLTIN(IV) COMPOUNDS | SILYL ENOL ETHERS | HOMOALLYLIC ALCOHOLS | CHEMISTRY, ORGANIC | X-RAY STRUCTURE | COORDINATED TIN(II) TRIFLATE
Journal Article
BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE, ISSN 0037-8968, 1993, Volume 130, Issue 3, pp. 388 - 394
Journal Article
Chemistry – An Asian Journal, ISSN 1861-4728, 09/2018, Volume 13, Issue 17, pp. 2164 - 2173
Journal Article
Coordination Chemistry Reviews, ISSN 0010-8545, 2002, Volume 235, Issue 1, pp. 1 - 52
This review deals with the recent progress in the area of organotin assemblies that contain Sn-O bonds. Various kinds of tri-, di- and monoorganotin compounds... 
Hydrolysis | Stannoxanes | Organotin compound | OXYGEN-CAPPED CLUSTER | PENTA-COORDINATED MOLECULES | X-RAY-DIFFRACTION | RECOIL-FREE FRACTION | MULTINUCLEAR NMR-SPECTROSCOPY | CHEMISTRY, INORGANIC & NUCLEAR | organotin compound | ORTHO-ANISIC ACID | stannoxanes | STATE SN-119 NMR | VITRO ANTITUMOR-ACTIVITY | ALCOHOL ACETYLATION CATALYSTS | DI-N-BUTYLTIN | hydrolysis
Journal Article
Coordination Chemistry Reviews, ISSN 0010-8545, 07/2014, Volume 270-271, Issue 1, pp. 57 - 74
Journal Article
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