1-naphthylboronic acid

COC(=O)[C@H](Cc1ccccc1)n1cc(-c2cccc3ccccc23)cc(NC(=O)c2ccc(C(F)(F)F)cc2)c1=O
Reaction #7903
title compound
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1cccc(-c2cccc3ccccc23)n1
Reaction #8237
2-formyl-6-naphthylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1nc(C)c(-c2cccc3ccccc23)s1
Reaction #40730
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCN(CC(c2ccc(Oc3cccc4ccccc34)cc2)C2(O)CCCCC2)CC1
Reaction #57121
tert-butyl 4-{2-(1-hydroxycyclohexyl)-2-[4-(1-naphthyloxy)phenyl]ethyl}piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1oc(N)nc1-c1cccc2ccccc12
Reaction #61854
5-methyl-4-naphthalen-1-yl-oxazol-2-ylamine
Yield 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN1CCN(c2ccc(NC(=O)c3ccc(-c4cccc5ccccc45)c4nccnc34)cc2)CC1
Reaction #71356
Title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N1CCC2c3cc(-c4cccc5ccccc45)cc4c3N(CCO4)C2CC1
Reaction #79333
tert-butyl 5-(1-naphthyl)-1,2,6b,7,8,10,11,11a-octahydro-9H-azepino[4,5-b][1,4]oxazino[2,3,4-hi]indole-9-carboxylate
Yield 268.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C1NC(=O)C(c2cn3c4c(cccc24)CCC3)=C1c1c[nH]c2ccc(-c3cccc4ccccc34)cc12
Reaction #91832
3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4(5-1-naphthyl-1H-indol-3-yl)pyrrole-2,5-dione
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)[C@H](C)Nc1cccc2ccccc12
Reaction #92518
title compound
Yield 34.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cnc(-c2cccc3ccccc23)c(C)n1
Reaction #157940
2-(1-naphthyl)-3,5-dimethylpyrazine
Yield 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(c1ccc(-c2cccc3ccccc23)cc1Cl)N1Cc2cccn2Cc2ccccc21
Reaction #245825
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)Cc1cccc2ccccc12
Reaction #262724
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=S(=O)(c1ccc(-c2cccc3ccccc23)s1)n1cccc1
Reaction #321645
N-[5-(1-napthyl)thiophene-2-sulfonyl]pyrrole
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(C)(C)c1nc(-c2ccc3ccccc3c2)c(-c2ccncc2)[nH]1
Reaction #357320
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=C1NC(=O)C(c2cn3c4c(cccc24)CCC3)=C1c1c[nH]c2ccc(-c3cccc4ccccc34)cc12
Reaction #372618
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1c2c(cccc2-c2cccc3ccccc23)CC1CC1CCCCC1
Reaction #394370
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Brc1ccc(-c2cccc3ccccc23)cc1
Reaction #405253
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1nc(N)nc(-c2cccc3ccccc23)c1C
Reaction #431027
2-amino-5,6-dimethyl-4-(naphth-1-yl)-pyrimidine
Yield 38.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CN1CCC[C@H]1COc1cncc(-c2cccc3ccccc23)c1
Reaction #452986
oil
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
O=C(N[C@@H](Cc1ccc(-c2cccc3ccccc23)cc1)C(=O)O)C(CS)Cc1ccccc1
Reaction #456383
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
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