Участвует в 4983 реакциях

4619

CCOC(=O)c1ccc(OCCN2CCCCC2)cc1
Reaction #2879
Ethyl 4-(2-Piperidinoethoxy)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(C)NCCNCC(C)(C)N
Reaction #3855
N-(2-butyl)-N'-(2-amino-2-methylpropyl)-1,2-ethanediamine
Выход 69.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1oc(-c2ccccc2)nc1C(=O)COc1ccc(C#N)cc1
Reaction #4507
4-[2-(5-methyl-2-phenyl-4-oxazolyl)-2-oxoethoxy]benzonitrile
Выход 79.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC1(C)CCC(C)(C)c2cc(OCc3ccc(C#N)cc3)ccc21
Reaction #6605
title compound
Выход 98.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)c1ccc(COc2ccc3c(c2)C(C)(C)CCC3(C)C)cc1
Reaction #6610
title compound
Выход 40.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(Cc1c[nH]c2c(OCC#N)cccc12)NC(=O)OC(C)(C)C
Reaction #8192
[2-(7-cyanomethoxy-1H-indol-3-yl)-1,1-dimethyl-ethyl]-carbamic acid tert-butyl ester
Выход 86.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(Cc1c[nH]c2c(OCC#N)cccc12)NC(=O)OC(C)(C)C
Reaction #8194
racemic {1-methyl-2-[7-cyanomethoxy-1H-indol-3-yl]ethyl}-carbamic acid tert-butyl ester
Выход 70.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)NS(=O)(=O)c1cccc2ccccc12
Reaction #8803
ethyl 1-naphthylsulfonylcarbamate
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.O=C(CCCN1CC(CS(=O)(=O)c2ccc(F)cc2)C1)c1ccc(F)cc1
Reaction #10301
1-(4-fluorophenyl)-4-(3-{[(4-fluorophenyl)sulfonyl]methyl}azetidin-1-yl)butan-1-one hydrochloride
Выход 6.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #11722
title compound
Выход 94.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #11728
title compound
Выход 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)Cc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11748
title compound
Выход 97.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1S(N)(=O)=O
Reaction #11759
title compound
Выход 70.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)CCCC(=O)c1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11808
title compound
Выход 47.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)C(Br)C(=O)c1cnc(NC(=O)C(C)(C)C)cn1
Reaction #40277
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCC.CCO
Reaction #41841
ethanol heptane
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
ICCOc1ccc(Cc2ccccc2)cc1
Reaction #44761
1-(2-iodoethoxy)-4-(benzyl)benzene
Выход 72.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
ICCOc1ccc(Cc2ccc(-c3ncco3)cc2)cc1
Reaction #44787
2-[4-[[4-(2-iodoethoxy)phenyl]methyl]phenyl]oxazole
Выход 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc2c(c3c1c(=O)c1cc4ccccc4nc1n3C)[C@H]1OC(=O)O[C@H]1C(C)(C)O2
Reaction #46315
(±)-cis-7-Methoxy-4,4,15-trimethyl-15,15c-dihydro-4H-benzo[b][1,3]-dioxolo[4′,5′:3,4]chromeno[6,5-g][1,8]naphthyridin-2,8[3aH]-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(CC(=O)c1ccc(Br)cc1)C(C)=O
Reaction #46917
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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