triethylborane

COc1cc(OC)c(-c2cc3ccccc3n2C)cc1C=O
Reaction #10839
2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)-benzaldehyde
収率 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCc1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12012
product
収率 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1(C)CCCCC1=O
Reaction #40310
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCc1cccc(CNC2CC2)c1
Reaction #42561
11
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCc1cccc(C#Cc2ccc(OC(F)F)cc2)c1
Reaction #58831
1-{[4-(difluoromethoxy)phenyl]ethynyl}-3-propylbenzene
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=CCC(C)(C=O)c1cc([N+](=O)[O-])ccc1F
Reaction #59103
2-(2-fluoro-5-nitrophenyl)-2-methylpent-4-enal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
NS(=O)(=O)c1ccc(-n2cc(C(F)(F)F)nc2-c2ccc(Cl)cc2)cc1
Reaction #80613
4-[2-(4-chlorophenyl)-4-(trifluoromethyl)-1H-imidazol-1-yl]benzenesulfonamide
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1ccc(-c2nc(C(F)(F)F)cn2-c2ccc(S(N)(=O)=O)cc2)cc1Cl
Reaction #80614
4-[2-(3-chloro-4-methylphenyl)-4-(trifluoromethyl)-1H-imidazol-1-yl]benzenesulfonamide
収率 36.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1ccc(-c2nc(C(F)(F)F)cn2-c2ccc(S(N)(=O)=O)cc2)cn1
Reaction #80632
4-[2-(6-methylpyridin-3-yl)-4-(trifluoromethyl)-1H-imidazol-1-yl]benzenesulfonamide
収率 12.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1cccc(-c2nc(C(F)(F)F)cn2-c2ccc(S(N)(=O)=O)cc2)n1
Reaction #80633
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1cncc(-c2nc(C(F)(F)F)cn2-c2ccc(S(N)(=O)=O)cc2)c1
Reaction #80641
4-[2-(5-methylpyridin-3-yl)-4-(trifluoromethyl) -1H-imidazol-1-yl]benzenesulfonamide
収率 9.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)C1CCn2c(C(=O)c3ccccc3)ccc21
Reaction #82180
5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid methyl ester
収率 62.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)C1CCn2c(C(=O)c3ccccc3)ccc21
Reaction #177846
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1OCCC1CCCCO
Reaction #178587
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cncc(-c2nc(C(F)(F)F)cn2-c2ccc(S(N)(=O)=O)cc2)c1
Reaction #199810
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1c(CC)cc(-c2c(CC)cccc2CC)nc1C
Reaction #230695
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)CC(O)CC(O)C=Cc1c(C)cc(C)cc1-c1ccc(F)c(C)c1
Reaction #245577
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCn1nc(-c2ccc(S(N)(=O)=O)cc2)c(-c2ccc(F)cc2)c1C(F)(F)F
Reaction #258800
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C(O)CC(O)CC(=O)OC(C)(C)C
Reaction #265447
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCc1cc(CO[Si](C)(C)C(C)(C)C)cc(NC(=O)OC(C)(C)C)n1
Reaction #265840
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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