Substructure Search

3807

COCOC(=O)c1cccc2c(CC(C)(C)NC(=O)OC(C)(C)C)c[nH]c12
Reaction #8221
[2-(7-(methoxycarbomethoxy)-1H-indol-3-yl)-1,1-dimethyl-ethyl]-carbamic acid tert-butyl ester
Yield 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2c(C(=O)OCNS(C)(=O)=O)cccc12)NC(=O)OC(C)(C)C
Reaction #8222
[2-(7-(methanesulfonamidylcarbomethoxy)-1H-indol-3-yl)-1,1-dimethyl-ethyl]-carbamic acid tert-butyl ester
Yield 117.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)c1cn(C(=O)OC(C)(C)C)c2ccccc12
Reaction #40497
3-(cyano-methyl-methyl)-indole-1-carboxylic acid tert-butyl ester
Yield 79.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1cn(C)c2ccc(C(=O)OCC)cc12
Reaction #42490
title compound
Yield 46.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1cn(C)c2ccc(C(=O)O)cc12
Reaction #42491
title compound
Yield 89.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Br)(Oc1cccc2[nH]ccc12)C(=O)OCC
Reaction #44843
7
Yield 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1cccc2[nH]ccc12)C(=O)OCC
Reaction #44844
8
Yield 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1cccc2[nH]ccc12)C(=O)OCC
Reaction #44849
8
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2cccc2C=O)cc1Cl
Reaction #52996
2-chloro-4-(2-formyl-1-pyrrolyl)benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc2c(cc1F)[nH]c1ccccc12
Reaction #78898
7-fluoro-6-nitro-carbazole
Yield 45.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1cc(Cl)cn1CCOC(C)=O
Reaction #95390
ethyl 1-(2-acetoxyethyl)4-chloropyrrole-2-glyoxalate
Yield 41.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #95392
Formula VI
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1cc(C)c(C(=O)OCC)[nH]1
Reaction #159955
title compound
Yield 47.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nn1cccc1C#N
Reaction #160867
desired product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #160868
white solid
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2cc(C(=O)O)n(Cc3ccc(Cl)cc3)c12
Reaction #170862
1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2cc(C(=O)N3CCC(C(=O)NCc4ccccc4)CC3)n(Cc3ccc(Cl)cc3)c12
Reaction #170863
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(NC(=O)c2cc3cc(F)ccc3n2Cc2cccc(F)c2)cn1
Reaction #176859
DOI: 10.1039/C8SC04228D
Cc1cccc(-n2ccc3c(CN4CCC(c5cccc(NC(=O)C(C)C)c5)CC4)cccc32)c1C
Reaction #178349
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #183056
DOI: 10.1039/C8SC04228D
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