Boronic acid

CC(C)(C)[Si](C)(C)Oc1cc2ccc(B(O)O)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #1240
7-(1-adamantyl)-6-tert-butyldimethylsilyloxy-2-naphthylboronic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ncc(-c2cccnc2F)c(OC)n1
Reaction #40990
title compound
Ausbeute 93.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCC[C@H]1c1nnc(-c2ccc(B(O)O)cc2)o1
Reaction #46630
(S)-4-(5-(1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-1,3,4-oxadiazol-2-yl)phenylboronic acid
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N[C@@H]1C[C@H]1c1ccc(-c2ccccc2)cc1
Reaction #66394
tert-butyl(trans)-2-(1,1′-biphenyl-4-yl)cyclopropylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ncc(-c2ccnc(Cl)n2)cc1C#N
Reaction #84143
desired compound
Ausbeute 51.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)N1CCN(C(=O)c2ccccc2F)C(COc2cccnc2)C1
Reaction #157372
tert-butyl 4-(2-fluorobenzoyl)-3-((pyridin-3-yloxy)methyl)piperazine-1-carboxylate
Ausbeute 28.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(-c2cc3c(cc2OC)N(C)C(=O)CN=C3c2cccc(C#N)c2)cc1
Reaction #173573
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc(C#Cc2ccnc(Cl)c2)cn1-c1ccc(Cl)cc1
Reaction #175500
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCOc1ccc(OC)c(-c2ccc(OC3CN(C(=O)Nc4cccnn4)C3)nc2)c1
Reaction #177338
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)S(=O)(=O)NCC(C)(F)c1ccc(-c2ccc(C(=O)O)cc2)cc1
Reaction #178309
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(-c2nc(Cl)nnc2C)ccc1OCc1ccccc1
Reaction #178583
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(-c2ccc(C(F)(F)F)cc2)nc(-c2ccnc(Cl)c2)c1
Reaction #178947
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSCc1ccc(N)c(-c2cccc(Cl)c2)c1
Reaction #181386
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)Cc1nc(-c2ccc(-c3ccc(S(C)(=O)=O)cc3)nc2)oc1C
Reaction #182536
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)Nc1ccc(-c2ccc(F)cc2F)cc1[N+](=O)[O-]
Reaction #182869
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1c(C=O)cc(S(N)(=O)=O)cc1-c1cccc(Cl)c1
Reaction #183060
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCS(=O)(=O)c1ccc(NC(=O)CCCc2ccc(B(O)O)cc2)cc1CNC(=O)OC(C)(C)C
Reaction #183265
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(-c2ccc(C(F)(F)F)nc2)cc(-c2cccc(Br)c2)n1
Reaction #183660
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=S(=O)(c1ccc(-c2ccc(C(F)(F)F)cc2)s1)n1cccc1
Reaction #183890
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)Nc1ccc(-c2cccc(F)c2F)cc1[N+](=O)[O-]
Reaction #184674
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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