X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (21344) 21344
Publication (689) 689
Book Chapter (204) 204
Book Review (169) 169
Conference Proceeding (43) 43
Dissertation (27) 27
Book / eBook (18) 18
Magazine Article (6) 6
Trade Publication Article (3) 3
Paper (2) 2
Data Set (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
multicomponent reactions (13515) 13515
chemistry, organic (4810) 4810
chemistry, multidisciplinary (3885) 3885
derivatives (3360) 3360
chemistry (2700) 2700
multicomponent reaction (2700) 2700
catalysis (2338) 2338
one-pot synthesis (2241) 2241
ring closure reactions (1706) 1706
aldehydes (1567) 1567
index medicus (1559) 1559
catalysis, phase‐transfer catalysis (1096) 1096
amines (1089) 1089
efficient synthesis (1080) 1080
pyridine (1072) 1072
heterocycles (1068) 1068
organic chemistry (1065) 1065
synthesis (1046) 1046
analysis (1039) 1039
efficient (932) 932
organic-synthesis (919) 919
multicomponent synthesis (888) 888
chemistry, physical (886) 886
engineering, chemical (872) 872
multicomponent (861) 861
catalysts (853) 853
chemical synthesis (818) 818
fused pyridine derivatives (813) 813
inhibitors (808) 808
ring closure reactions, annulation reactions (770) 770
chemistry, applied (751) 751
cyclization (741) 741
green chemistry (704) 704
molecular structure (694) 694
diastereoselective syntheses, enantioselective syntheses (682) 682
water (678) 678
solvent-free conditions (655) 655
nanoparticles (621) 621
fused pyrimidine derivatives (620) 620
acid (616) 616
one-pot (612) 612
chemistry, medicinal (585) 585
condensation (581) 581
microwave chemistry, sonochemistry, mechanochemistry (577) 577
organocatalysis (572) 572
copper (563) 563
ketones (554) 554
physical chemistry (549) 549
pyridine derivatives (524) 524
isocyanides (519) 519
cycloaddition (518) 518
alkynes (517) 517
nitriles (517) 517
design (504) 504
inorganic chemistry (504) 504
indole derivatives, isoindole derivatives (498) 498
benzopyran derivatives (497) 497
materials science, multidisciplinary (491) 491
palladium (487) 487
thermodynamics (476) 476
pyrimidine derivatives (472) 472
catalyst (471) 471
alkaloids (469) 469
heterocyclic compounds (466) 466
cycloaddition reactions (457) 457
chemical properties (456) 456
stereoselective-synthesis (447) 447
3-component synthesis (444) 444
solvent-free (432) 432
spirocyclic compounds (432) 432
facile synthesis (428) 428
ionic liquid (420) 420
3-component reaction (417) 417
domino reactions (417) 417
chemistry, inorganic & nuclear (414) 414
drug discovery (404) 404
solvents (385) 385
chemical reactions (383) 383
stereoisomerism (380) 380
pyrrole derivatives (376) 376
letter (370) 370
humans (366) 366
agents (361) 361
discovery (358) 358
isocyanide (347) 347
pyrimidines (347) 347
esters (345) 345
reusable catalyst (344) 344
quinoline derivatives (342) 342
pyran derivatives (339) 339
pyrazole derivatives (338) 338
tetrahedrons (337) 337
asymmetric-synthesis (336) 336
construction (334) 334
terminal alkynes (333) 333
heterogeneous catalyst (329) 329
oxidation (329) 329
acids (328) 328
biological evaluation (326) 326
diffusion (326) 326
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (21441) 21441
Chinese (86) 86
Japanese (19) 19
German (16) 16
Portuguese (10) 10
Spanish (7) 7
French (6) 6
Korean (5) 5
Catalan (1) 1
Czech (1) 1
Russian (1) 1
more...
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, 01/2011, Volume 50, Issue 3, pp. 644 - 649
Journal Article
Synthesis, ISSN 0039-7881, 01/2014, Volume 46, Issue 2, pp. 135 - 157
Abstract The Povarov reaction provides a straightforward and modular entry to 1,2,3,4-tetrahydroquinolines (THQs). Despite its importance, it was only very... 
review | imines | cycloaddition | asymmetric catalysis | multicomponent reaction | heterocycles | ENANTIOSELECTIVE SYNTHESIS | LEWIS-ACID | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | N-ARYL IMINES | TETRAHYDROQUINOLINE DERIVATIVES | MANNICH-TYPE REACTION | MULTICOMPONENT COUPLING REACTION | PHOSPHORIC-ACID | QUINOLINE DERIVATIVES | CHIRAL BRONSTED ACID
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 08/2017, Volume 2017, Issue 30, pp. 4379 - 4388
A one‐pot procedure involving a four‐component Ugi reaction followed by an intramolecular Diels–Alder reaction/HCl elimination cascade has been developed to... 
Domino reactions | Cycloaddition | Multicomponent reactions | Nitrogen heterocycles | Ugi reaction | Diels–Alder reaction | SEQUENTIAL UGI | GOLD | CASCADE REACTIONS | CHEMISTRY, ORGANIC | DIVERSE HETEROCYCLIC SCAFFOLDS | PASSERINI REACTIONS | ORIENTED SYNTHESIS | WITTIG REACTION | Diels-Alder reaction | BETA-LACTAMS | WATER | Analysis
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 11/2016, Volume 57, Issue 47, pp. 5135 - 5149
Biginelli reaction involves acid-catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2(1 )-ones (DHPMs) using easily-accessible starting materials, namely,... 
Urea | Active methylene compound | Biginelli reaction | Dihydropyrimidinones | Multicomponent reaction | Aldehyde | ASYMMETRIC-SYNTHESIS | POLYCYCLIC GUANIDINE ALKALOIDS | SMALL-MOLECULE | CHEMISTRY, ORGANIC | SPONGE CRAMBE-CRAMBE | CALCIUM-CHANNEL BLOCKERS | IN-VITRO | POTENT | ANTITUBERCULAR ACTIVITY | IONIC LIQUIDS | ACID-ESTERS
Journal Article
Organic Letters, ISSN 1523-7060, 05/2006, Volume 8, Issue 11, pp. 2245 - 2248
A novel and efficient carbon−carbon double-bond formation reaction via coupling of aryl or heteroaryl methyl ketones has been developed. A dimethyl... 
OXIDATION | MULTICOMPONENT REACTIONS | ORGANIC-SYNTHESIS | DOMINO REACTIONS | CATALYTIC-REDUCTION | DIMETHYL SULFOXIDE | ACID SYSTEM | CYCLOADDITIONS | CHEMISTRY, ORGANIC | PYRROLE SYNTHESIS | TRANSFORMATIONS
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 04/2017, Volume 58, Issue 16, pp. 1640 - 1643
A series of compounds containing the benzoxazepine-isoquinoline scaffold was synthesized in a one-pot procedure via an Ugi reaction followed by tautomerization... 
Isoquinoline | Multicomponent reaction | Nucleophilic substitution reaction | One-pot operation | Benzoxazepine | ENTRY | ONE-POT | ARYLATION | UDC STRATEGY | CHEMISTRY, ORGANIC | MULTICOMPONENT REACTIONS | CHEMISTRY | INHIBITORS | SCAFFOLDS | FACILE | WATER | Alkaloids | Synthesis | Organic compounds
Journal Article
Organic Letters, ISSN 1523-7060, 04/2007, Volume 9, Issue 9, pp. 1687 - 1690
Journal Article
Journal Article