MnO2

O=Cc1cccc(Oc2ccccc2)c1
Reaction #976
aldehyde
Выход 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #1398
4,4'-difluorobenzophenone
Выход 69.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #1399
4,4'-difluorobenzophenone
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #1400
4,4'-difluorobenzophenone
Выход 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C=O)cc1I
Reaction #3069
3-iodo-4-methylbenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc2ccccc21
Reaction #6800
N-methyl indole
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cccnc1C=O
Reaction #7240
3-methylpyridine-2-carboxaldehyde
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCOc1cccnc1C=O
Reaction #7241
3-n-propoxypyridine-2-carboxaldehyde
Выход 113.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N(Cc1ccc(C=O)cc1)Cc1ncccc1O
Reaction #7288
crystals
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)NCCc1ccc(C=O)cc1
Reaction #9007
aldehyde
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)NC(=Nc1ccc(C=O)cc1)NC(=O)OC(C)(C)C
Reaction #9045
N, N′-bis-(tert-butoxycarbonyl)-N″-(4-formyl-phenyl)-guanidine
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1ccc(-c2nc3ccccc3[nH]2)cc1
Reaction #9064
4-(benzimidazol-2-yl)-benzaldehyde
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1ccc(-c2cnco2)cc1
Reaction #9073
aldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc2c(c1)c1c3c(c(-c4ccccc4Cl)cc1n2CCO)C(=O)NC3=O
Reaction #11137
4-(2-Chlorophenyl)-6-(2-hydroxyethyl)-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(Br)c2oc3cc(-c4ccccc4Cl)c4c(c3c2c1)C(=O)NC4=O
Reaction #11249
dibenzofuran
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41803
2
Выход 94.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1cnc(CN2C(=O)c3ccccc3C2=O)c2c(OC)cc(OC)cc12
Reaction #42904
1-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-6,8-dimethoxy-isoquinoline-4-carboxylic acid ethyl ester
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1ccc2c(c1)N=Cc1ccccc1N2
Reaction #44469
title compound
Выход 102.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)c1cc(NC(=O)Nc2cccc3ccccc23)n(-c2ccc(C=O)cc2)n1
Reaction #45261
1-[5-t-butyl-2-(4-formyl-phenyl)-2H-pyrazol-3-yl]-3-naphthalen-1-yl-urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ncc(C=O)c2scc(Br)c12
Reaction #45429
desired product
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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