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CC1(C)OB(c2ccc(Cl)nc2)OC1(C)C

CNc1ccc(B2OC(C)(C)C(C)(C)O2)cn1
Reaction #85801
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(B2OC(C)(C)C(C)(C)O2)cn1
Reaction #85802
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OB(O)c1ccc(N2CCC(O)C2)nc1
Reaction #85826
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCC(c2cc(N(COCC[Si](C)(C)C)COCC[Si](C)(C)C)n3ncc(-c4ccc(Cl)nc4)c3n2)CC1
Reaction #173407
DOI: 10.1039/C8SC04228D
CC(=O)Nc1cc(-c2ccc3ncc4c(c3c2)n(-c2cn(C)nc2C)c(=O)n4C)cnc1Cl
Reaction #174394
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)Nc2cc(-c3ccc4nc(NC(C)C)sc4c3)cnc2Cl)cc1
Reaction #203110
DOI: 10.1039/C8SC04228D
O=S(=O)(Nc1cc(-c2ccc3ncc(Cl)nc3c2)cnc1Cl)c1ccc(F)cc1
Reaction #205205
DOI: 10.1039/C8SC04228D
O=S(=O)(Nc1cc(-c2ccc3c(c2)OCCO3)cnc1Cl)c1ccc(F)cc1
Reaction #257463
DOI: 10.1039/C8SC04228D
O=c1c2cccnc2ccn1-c1cnc(Cl)c(NS(=O)(=O)c2ccc(F)cc2)c1
Reaction #374164
DOI: 10.1039/C8SC04228D
Clc1ccc(Cl)c(CN2CCNc3ncc(-c4ccc(Cl)nc4)cc32)c1
Reaction #387077
DOI: 10.1039/C8SC04228D
O=S(=O)(Nc1cc(-c2ccnc3cccnc23)cnc1Cl)c1ccc(F)cc1
Reaction #397608
DOI: 10.1039/C8SC04228D
Cc1nn(C(C)C)cc1-n1c(=O)n(C)c2cnc3ccc(-c4cnc(Cl)c(N)c4)cc3c21
Reaction #532885
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1cc(-c2ccc3ncc4c(c3c2)n(-c2c(C)nn(C)c2C)c(=O)n4C)cnc1Cl
Reaction #532887
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(-c2ccc3ncc4c(c3c2)n(-c2cn(C)nc2C)c(=O)n4C)cnc1Cl
Reaction #532939
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(C)cc1-n1c(=O)n(C)c2cnc3ccc(-c4cnc(Cl)c(NS(C)(=O)=O)c4)cc3c21
Reaction #532941
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(B2OC(C)(C)C(C)(C)O2)cnc(Cl)c1F
Reaction #556114
boronic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)cncc1B1OC(C)(C)C(C)(C)O1
Reaction #556115
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)c(B2OC(C)(C)C(C)(C)O2)cn1
Reaction #556122
title compound
Rendimiento 64.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2ccc(F)cc2F)c(-c2cnc(Cl)cc2F)c1
Reaction #605531
2-chloro-5-[2-(2,4-difluorophenoxy)-5-nitrophenyl]-4-fluoropyridine
Rendimiento 57.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2ccc(F)cc2F)c(-c2cnc(Cl)cc2F)c1
Reaction #662801
2-chloro-5-[2-(2,4-difluorophenoxy)-5-nitrophenyl]-4-fluoropyridine
Rendimiento 57.3%DOI: 10.6084/m9.figshare.5104873.v1
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