Substructure Search

OB(O)c1cccc2ccccc12

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.v1
O=Cc1cccc(-c2cccc3ccccc23)n1
Reaction #8237
2-formyl-6-naphthylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(C)c(-c2cccc3ccccc23)s1
Reaction #40730
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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.v1
Cc1oc(N)nc1-c1cccc2ccccc12
Reaction #61854
5-methyl-4-naphthalen-1-yl-oxazol-2-ylamine
Yield 14.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(NC(=O)c3ccc(-c4cccc5ccccc45)c4nccnc34)cc2)CC1
Reaction #71356
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Sc1ncccc1-c1ccc(C#N)c2ccccc12
Reaction #74056
ethyl 2-(3-(4-cyanonaphthalen-1-yl)pyridin-2-ylthio)-2-methylpropanoate
Yield 36.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2nccnc2Cl)c2ccccc12
Reaction #74058
4-(3-chloropyrazin-2-yl)-1-naphthonitrile
Yield 242.8%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2cncnc2SCC(=O)O)c2ccccc12
Reaction #74062
2-(5-(4-cyanonaphthalen-1-yl)pyrimidin-4-ylthio)acetic acid
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ncncc2Br)c2ccccc12
Reaction #74063
4-(5-bromopyrimidin-4-yl)-1-naphthonitrile
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1
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.v1
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.v1
COC(=O)[C@H](C)Nc1cccc2ccccc12
Reaction #92518
title compound
Yield 34.1%DOI: 10.6084/m9.figshare.5104873.v1
OB(O)c1cccc2c1ccc1ccccc12
Reaction #155687
phenanthrene-1-boronic acid
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(-c2cccc3c2ccc2ccccc23)cc1
Reaction #155688
1-(4-bromophenyl)phenanthrene
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cccc(-c2ccc3ccc4ccccc4c3c2)c1
Reaction #155689
3-(3-bromophenyl)phenanthrene
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2cc(-c3cccc4c3ccc3ccccc34)ccc2c1
Reaction #155692
1-(6-bromonaphthalene-2-yl)phenanthrene
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(-c2cccc3ccccc23)c(C)n1
Reaction #157940
2-(1-naphthyl)-3,5-dimethylpyrazine
Yield 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1
Reaction #159021
pyrrolidine-1-carboxylic acid tert-butyl ester
Yield 87.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(-c3cnnc(Cn4ccnc4C)c3)cccc2c1
Reaction #208677
DOI: 10.1039/C8SC04228D
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