X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
1,3-dipolar cycloaddition (4970) 4970
chemistry, organic (4956) 4956
chemistry, multidisciplinary (2563) 2563
1,3-dipolar cycloadditions (2083) 2083
derivatives (1789) 1789
cycloaddition (1382) 1382
chemistry (1315) 1315
index medicus (1267) 1267
click chemistry (1107) 1107
catalysis (953) 953
azomethine ylides (927) 927
terminal alkynes (927) 927
1,3-dipolar cycloaddition reactions (829) 829
synthesis (648) 648
azides (637) 637
organic chemistry (615) 615
molecular structure (614) 614
chemistry, inorganic & nuclear (584) 584
cyclization (577) 577
one-pot synthesis (570) 570
nitrones (530) 530
analysis (526) 526
alkynes (523) 523
chemistry, physical (519) 519
stereoisomerism (519) 519
diels-alder reactions (508) 508
heterocycles (504) 504
chemical properties (465) 465
chemistry, medicinal (438) 438
stereoselective-synthesis (437) 437
triazoles (427) 427
copper (407) 407
organic-synthesis (407) 407
regioselectivity (403) 403
inhibitors (397) 397
asymmetric-synthesis (395) 395
efficient synthesis (394) 394
diels-alder reaction (390) 390
reactivity (387) 387
azide-alkyne cycloaddition (382) 382
enantioselective synthesis (376) 376
nitrile oxides (368) 368
regioselective synthesis (355) 355
construction (342) 342
ligands (334) 334
biochemistry & molecular biology (324) 324
1,3-dipolar cycloaddition reaction (318) 318
aldehydes (317) 317
analogs (315) 315
catalysts (314) 314
1,2,3-triazoles (309) 309
chemistry, applied (299) 299
schiff bases (299) 299
complexes (294) 294
esters (288) 288
chemical synthesis (286) 286
alkaloids (285) 285
alkenes (274) 274
efficient (266) 266
research (265) 265
ligation (263) 263
acid (258) 258
zykloaddition (253) 253
azomethine ylide (242) 242
triazole (236) 236
imines (235) 235
design (233) 233
alkynes - chemistry (232) 232
humans (228) 228
polymer science (228) 228
biological evaluation (227) 227
asymmetric catalysis (225) 225
mechanism (221) 221
route (221) 221
polymers (220) 220
ring formation (218) 218
stereoselectivity (218) 218
azide (216) 216
ketones (216) 216
chemical reactions (215) 215
models, molecular (215) 215
click-chemistry (214) 214
one-pot (209) 209
asymmetric 1,3-dipolar cycloaddition (208) 208
azides - chemistry (207) 207
amino-acids (205) 205
multicomponent reactions (204) 204
ylides (204) 204
article (198) 198
nitriles (196) 196
enantioselective 1,3-dipolar cycloaddition (195) 195
cycloadditions (192) 192
cycloaddition reaction (191) 191
huisgen 1,3-dipolar cycloaddition (190) 190
oxidation (189) 189
letter (186) 186
facile synthesis (185) 185
tetrahedrons (183) 183
1,4-disubstituted 1,2,3-triazoles (181) 181
chemical sciences (178) 178
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (9303) 9303
Chinese (133) 133
Japanese (130) 130
German (41) 41
French (39) 39
Russian (34) 34
Czech (1) 1
Malay (1) 1
Polish (1) 1
Portuguese (1) 1
Romanian (1) 1
Spanish (1) 1
Welsh (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Accounts of Chemical Research, ISSN 0001-4842, 10/2017, Volume 50, Issue 10, pp. 2621 - 2631
Conspectus Catalytic asymmetric cycloadditions and cascade cyclizations are a major focus for the enantioselective construction of chiral carbo- and... 
HIGHLY ENANTIOSELECTIVE SYNTHESIS | C BOND-CLEAVAGE | BRASSARD-TYPE DIENE | CYCLOPROPYL KETONES | DIELS-ALDER REACTION | 1,3-DIPOLAR CYCLOADDITION | EFFICIENT SYNTHESIS | BETA,GAMMA-UNSATURATED ALPHA-KETOESTERS | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | AZOMETHINE IMINES
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 11/2015, Volume 137, Issue 43, pp. 13938 - 13942
Heterocyclic skeletons are widespread among natural products as well as bioactive molecules. Cycloaddition reaction has created new opportunities to access... 
GOLD | ORGANIC-MOLECULES | EFFICIENT 1,2-DEHYDROCARBORANE PRECURSOR | REACTIVITY | STRUCTURAL-CHARACTERIZATION | CARBORANES | DIASTEREOSELECTIVE 1,3-DIPOLAR CYCLOADDITION | GENERATION | ARYNES | CHEMISTRY, MULTIDISCIPLINARY | NITRENIUM IONS
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 2010, Volume 39, Issue 5, pp. 1467 - 1477
Cycloaddition reactions belong to one of the most well-investigated and widely used reactions in synthetic organic chemistry for the construction of (hetero)... 
CORE | 1,3-DIPOLAR CYCLOADDITIONS | AZIDES | ANALOG | PINNAIC ACID | CLICK CHEMISTRY | TERMINAL ALKYNES | CASCADE | TIAZOFURIN | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 2010, Volume 39, Issue 5, pp. 1467 - 1477
Cycloaddition reactions belong to one of the most well-investigated and widely used reactions in synthetic organic chemistry for the construction of (hetero)... 
CORE | 1,3-DIPOLAR CYCLOADDITIONS | AZIDES | ANALOG | PINNAIC ACID | CLICK CHEMISTRY | TERMINAL ALKYNES | CASCADE | TIAZOFURIN | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Organic Letters, ISSN 1523-7060, 10/2016, Volume 18, Issue 19, pp. 4774 - 4777
A highly enantioselective 1,3-dipolar cycloaddition of imino esters with methyleneindolinones has been realized by using readily available thiourea–quaternary... 
AZA-HENRY REACTION | PHOSPHONIUM SALTS | LEWIS-ACID | NATURAL-PRODUCTS | DUAL-REAGENT CATALYSIS | PHASE-TRANSFER CATALYSIS | AZOMETHINE YLIDES | CHEMISTRY, ORGANIC | ALPHA-AMINO-ACIDS | ENANTIOSELECTIVE 1,3-DIPOLAR CYCLOADDITION | MICHAEL REACTIONS
Journal Article
Angewandte Chemie - International Edition, ISSN 0570-0833, 2009, Volume 48, Issue 27, pp. 4900 - 4908
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 01/2019, Volume 2019, Issue 2-3, pp. 391 - 400
Journal Article