X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
chemistry, organic (905) 905
chemistry, multidisciplinary (499) 499
baylis-hillman adducts (496) 496
baylis-hillman reaction (468) 468
derivatives (406) 406
adducts (266) 266
aldehydes (248) 248
catalysis (241) 241
stereoselective-synthesis (200) 200
acetates (175) 175
chemistry (171) 171
index medicus (148) 148
organocatalysis (138) 138
synthesis (130) 130
cyclization (129) 129
esters (125) 125
morita-baylis-hillman (122) 122
construction (121) 121
one-pot synthesis (118) 118
enantioselective synthesis (115) 115
asymmetric-synthesis (114) 114
acid (110) 110
facile synthesis (106) 106
baylis–hillman adducts (104) 104
michael addition (102) 102
efficient synthesis (96) 96
stereoisomerism (94) 94
ketones (89) 89
organic chemistry (89) 89
molecular structure (87) 87
asymmetric catalysis (85) 85
palladium (84) 84
catalysts (83) 83
baylis-hillman adduct (82) 82
cycloaddition (81) 81
morita-baylis-hillman reaction (80) 80
화학 (79) 79
morita-baylis-hillman adducts (78) 78
efficient (76) 76
inhibitors (76) 76
baylis-hillman (73) 73
conjugate addition (73) 73
alcohols (71) 71
baylis–hillman reaction (69) 69
organic-synthesis (68) 68
mechanism (67) 67
heterocycles (65) 65
chemistry, applied (64) 64
route (63) 63
chemistry, medicinal (62) 62
letter (60) 60
methyl vinyl ketone (60) 60
regioselective synthesis (60) 60
alkylation (59) 59
facile (59) 59
diels-alder reactions (58) 58
convenient synthesis (53) 53
n-sulfonated imines (53) 53
chemistry, physical (52) 52
amines (51) 51
substitution (51) 51
enantiomers (49) 49
analysis (48) 48
carbonyl-compounds (47) 47
tetrahedrons (47) 47
chemical properties (46) 46
imines (46) 46
chemical reactions (45) 45
acids (44) 44
alkaloids (44) 44
asymmetric synthesis (44) 44
chemical synthesis (44) 44
rearrangement (44) 44
alkenes (42) 42
asymmetry (42) 42
isomerization (42) 42
oxidation (42) 42
friedel-crafts reaction (41) 41
kinetic resolution (41) 41
baylis-hillman acetates (40) 40
dabco (40) 40
morita–baylis–hillman adducts (40) 40
olefins (40) 40
rate acceleration (40) 40
activated olefins (39) 39
conversion (39) 39
analogs (38) 38
baylis-hillman carbonates (38) 38
morita–baylis–hillman (38) 38
organic compounds (38) 38
stereoselectivity (38) 38
annulation (37) 37
lewis base (37) 37
biological evaluation (36) 36
heck reaction (36) 36
morita–baylis–hillman reaction (36) 36
strategy (36) 36
1,3-dipolar cycloaddition (35) 35
aldol reaction (35) 35
titanium chloride (35) 35
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1674) 1674
Japanese (14) 14
Chinese (10) 10
Portuguese (8) 8
Croatian (1) 1
French (1) 1
German (1) 1
Spanish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Chemistry Letters, ISSN 0366-7022, 12/2017, Volume 46, Issue 12, pp. 1718 - 1720
The oxa-Michael addition of Morita–Baylis–Hillman adducts and derivatives has been investigated for the first time to afford various types of polymeric... 
S | Morita–Baylis–Hillman adduct | Oxa-Michael addition | 2′ reaction | ALCOHOLS | POLYMERS | Morita-Baylis-Hillman adduct | DEGRADATION | S(N)2' reaction | ALDEHYDES | CONTROLLED CATIONIC COPOLYMERIZATION | CHEMISTRY, MULTIDISCIPLINARY | VINYL ETHERS | ACRYLATES | Addition polymerization | Polymerization | Chemical reactions | Derivatives | Dehydration | Aldehydes | Michael reaction | Adducts
Journal Article
ACS Catalysis, ISSN 2155-5435, 09/2011, Volume 1, Issue 9, pp. 989 - 993
Journal Article
Synthesis (Stuttgart), ISSN 0039-7881, 2017, Volume 49, Issue 24, pp. 5371 - 5379
Azides obtained from Baylis–Hillman adducts were treated with triphenylphosphine to give the corresponding iminophosphoranes, which reacted with carbon disulfide at 40... 
paper | isothiocyanates | Baylis-Hillman adducts | 2-thioxo-2,3-dihydropyrimidin-4(1H)-ones | aza-Wittig reaction | iminophosphoranes | primary amines | INHIBITORY-ACTIVITY | CHEMISTRY, ORGANIC | CARBOXYLIC-ACID | PYRIMIDINONE DERIVATIVES | PRIMARY AMINE | 4-COMPONENT SYNTHESIS | BIOLOGICAL EVALUATION | N-ISOCYANIMINOTRIPHENYLPHOSPHORANE | IMINOPHOSPHORANE | 1,3,4-OXADIAZOLES
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 01/2018, Volume 24, Issue 5, pp. 1204 - 1208
Journal Article
Molecules, ISSN 1420-3049, 02/2017, Volume 22, Issue 2, pp. 207 - 207
Journal Article
Synlett, ISSN 0936-5214, 05/2015, Volume 26, Issue 8, pp. 1026 - 1030
Abstract A copper-catalyzed γ-cyanation of aza-Baylis–Hillman adducts via iminium ion formation adjacent to benzylic tertiary amines has been developed using tert -butyl hydroperoxide (TBHP... 
letter | Michael addition | Baylis-Hillman adducts | copper catalysis | electron transfer | benzylic amines | cyanides | SP C-H | ACTIVATION | TETRAHYDROISOQUINOLINES | VISIBLE-LIGHT PHOTOREDOX | CHEMISTRY, ORGANIC | BOND FORMATION | IONIC LIQUID | ALKYNYLATION | DEHYDROGENATIVE-COUPLING CDC | DUAL CATALYSIS | CYCLIZATION
Journal Article
Synlett, ISSN 0936-5214, 06/2017, Volume 28, Issue 9, pp. 1075 - 1078
Abstract Iminophosphoranes reacted with CS 2 at –5 °C to produce the isothiocyanates, which were treated with primary amine to give thioureas in 73–91% yields.... 
letter | isothiocyanate | aza-Wittig reaction | pyrimidin-4(3 H)-one | Baylis-Hillman reaction | isomerization | ROUTE | AZIDES | VIRUS | pyrimidin-4(3H)-one | ONE-POT SYNTHESIS | REVERSE-TRANSCRIPTASE | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | SEQUENCE | ACETATES | INHIBITORS | DERIVATIVES
Journal Article
Comptes rendus - Chimie, ISSN 1631-0748, 05/2017, Volume 20, Issue 5, pp. 484 - 491
An efficient nucleophilic allylic substitution of a variety of Morita–Baylis–Hillman adducts with enamines catalyzed by Pd(OAc... 
1,5-Dicarbonyl compounds | Conjugate addition | Palladium | Allylic substitution | Enamine | Morita–Baylis–Hillman | KETONES | Morita-Baylis-Hillman | ESTERS | ACETATES | CHEMISTRY, MULTIDISCIPLINARY | Acetates
Journal Article
Synthesis, ISSN 0039-7881, 01/2015, Volume 47, Issue 1, pp. 113 - 123
...-amino esters from Morita–Baylis–Hillman (MBH) adducts is described. The strategy is based on a one-pot sequence involving an oxidative cleavage of the double bond of silylated Morita–Baylis... 
paper | Morita-Baylis-Hillman adducts | diastereoselectivity | DOPA | reduction | amino acids | ASYMMETRIC-SYNTHESIS | ENANTIOSELECTIVE SYNTHESIS | MOLECULAR-ORBITAL METHODS | CHEMISTRY, ORGANIC | IRELAND-CLAISEN REARRANGEMENT | GAUSSIAN-TYPE BASIS | L-DOPA PRODUCTION | DYNAMIC KINETIC RESOLUTION | ACID-DERIVATIVES | SPHINGOFUNGIN-E | HETEROGENEOUS CATALYTIC-HYDROGENATION
Journal Article
Bulletin of the Korean Chemical Society, ISSN 0253-2964, 10/2005, Volume 26, Issue 10, pp. 1481 - 1490
Journal Article
Synthesis, ISSN 0039-7881, 10/2013, Volume 45, Issue 20, pp. 2867 - 2874
...–Hillman adducts for the synthesis of highly functionalized α-benzyl-β-keto ester derivatives in good to excellent yields has been developed... 
paper | Heck reaction | α-benzyl-β-keto esters | Baylis-Hillman adducts | palladium | desulfitative | EFFICIENT APPROACH | CHEMISTRY, ORGANIC | BOND FORMATION | ARENESULFONYL CHLORIDES | CROSS-COUPLINGS | PALLADIUM-CATALYZED REACTIONS | C-C | benzyl--keto esters | STEREOSELECTIVE-SYNTHESIS | PD-MEDIATED SYNTHESIS | SULFONYL CHLORIDES | CONJUGATE ADDITION
Journal Article