参与 322 个反应

11541

COC(=O)c1ccccc1-c1ccc(C#N)cc1
Reaction #10166
methyl 4′-cyano-1,1′-biphenyl-2-carboxylate
收率 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1cc(Cl)nc(CC(C)=O)c1
Reaction #819580
title compound
收率 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CC(Nc1ccccc1)C(=O)O
Reaction #987815
title compound
收率 45.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
COc1ccccc1-c1c(Cl)cccc1Cl
Reaction #989480
2′,6′-dichloro-1,1′-biphenyl-2-yl methyl ether
收率 49.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
Cc1ccc(S(=O)(=O)OCC2CCc3cc(F)cc(-c4ccccc4Cl)c3O2)cc1
Reaction #989494
toluene-4-sulfonic acid 8-(2-chloro-phenyl)-6-fluoro-chroman-2-ylmethyl ester
收率 71.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
Cc1ccc(S(=O)(=O)OCC2C=Cc3cc(F)cc(-c4ccccc4Cl)c3O2)cc1
Reaction #989510
[8-(2-chlorophenyl)-6-fluoro-2H-chromen-2-yl]methyl 4-methylbenzenesulfonate
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
CC(OCC1(c2ccc(F)cc2)CCN(C(=O)OC(C)(C)C)CC1)c1cc(N(C)C)cc2cn(COCC[Si](C)(C)C)nc12
Reaction #1001037
(±)-tert-Butyl 4-((1-(5-dimethylamino-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-7-yl)ethoxy)methyl)-4-(4-fluorophenyl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
Cc1cc2cnn(-c3ccccc3)c2nc1OCc1ncnn1C
Reaction #1350673
title compound
收率 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
Cc1ccccc1P(c1ccccc1C)c1ccccc1C.Cc1ccccc1P(c1ccccc1C)c1ccccc1C.[Cl][Pd][Cl]
Reaction #1364725
bis[tri(ortho-tolyl)phosphine] palladium chloride
收率 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_07
COC(=O)c1cc(Cl)nc(CC(C)=O)c1
Reaction #1523724
title compound
收率 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11
COC(=O)CC1CCc2cc(N3CCCCC3)cc3[nH]c(=O)c(=O)n1c23
Reaction #2025011
收率 0.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
CCOC(=O)c1ncn2c1CN(C)C(=O)c1cc(N3CCCCC3)ccc1-2
Reaction #2025012
收率 0.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
CC1(C)OC(=O)C(Oc2ccc(N3CCCCC3)cn2)=C1c1ccc(S(C)(=O)=O)cc1
Reaction #2025013
收率 0.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
COC(=O)[C@@H]1C[C@@H](OC(=O)N2Cc3c(F)ccc(N4CCCCC4)c3C2)CN1C(=O)OC(C)(C)C
Reaction #2025014
收率 0.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
O=C(c1c[nH]c2ccc(N3CCCCC3)cc12)[C@@H]1CCCN1C(=O)OCc1ccccc1
Reaction #2025015
收率 0.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
CCOC(=O)N1CCC(=C2c3ccc(Cl)cc3CCc3cc(N4CCCCC4)cnc32)CC1
Reaction #2025016
收率 7.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
O=C(O)C[C@H]1CCc2c1n(Cc1ccc(Cl)cc1)c1c(N3CCCCC3)cc(F)cc21
Reaction #2025017
收率 0.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
COC(=O)[C@@H]1C[C@@H](OC(=O)N2Cc3cccc(N4CCCCC4)c3C2)CN1C(=O)OCc1ccccc1
Reaction #2025018
收率 0.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
O=C(O)Cn1nnc(-c2cc(N3CCC(Oc4cc(F)ccc4N4CCCCC4)CC3)no2)n1
Reaction #2025019
收率 0.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
O=C(NCc1ccc(F)cc1)c1nc(N2CCCCC2)c2cccnc2c1O
Reaction #2025020
收率 15.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
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