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C=O

CCNC(=O)Nc1nc2c(s1)C(=O)CCC2
Reaction #9202
4
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H]3c4ccc(O)cc4CC[C@H]3[C@@H]1CC[C@@H]2O
Reaction #50911
estradiol
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)NC(=O)C3=Cc2[nH]c3c(c2CCC(=O)O)CCCC3)c1
Reaction #52793
3-{2-[6-(3-methoxyphenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-4,5,6,7-tetrahydro-1H-indol-3-yl}-propionic acid
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc3c(c2)NC(=O)C3=Cc2[nH]c3c(c2CCC(=O)O)CCCC3)cc1
Reaction #52794
3-{2-[6-(4-Methoxyphenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-4,5,6,7-tetrahydro-1H-indol-3-yl}-propionic acid
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1c(C=C2C(=O)Nc3cc(-c4ccccc4)ccc32)[nH]c2c1CCCC2
Reaction #52795
3-[2-(2-oxo-6-phenyl-1,2-dihydro-indol-3-ylidenemethyl)-4,5,6,7-tetrahydro-1H-indol-3yl]-propionic acid
Ausbeute 33.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](CC(=O)OCc1ccccc1)C(=O)N[C@H](C(=O)N[C@@H](COCc1ccccc1)C(=O)N[C@@H](COCc1ccccc1)C(=O)N[C@@H](CCC(=O)OCc1ccccc1)C(=O)O)[C@@H](C)OCc1ccccc1
Reaction #54611
Boc-Val-Asp(OBzl)-Thr(Bzl)-Ser(Bzl)-Ser(Bzl)-Glu(OBzl)-OH
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C1(C)CC(=O)N(C)C1(O)CC2
Reaction #54673
3,9b-Dimethyl-3a-hydroxy-8-methoxy-2-oxo-2,3,3a,4,5,9b-hexahydro-1H-benz[e]indole
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1sc(N(C)C)nc1C
Reaction #60640
1-(2-dimethylamino-4-methyl-thiazol-5-yl)-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(CC(O)COCCOCC(O)CN(C(C)=O)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I
Reaction #70107
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1sc(NC(=O)c2ccc(Cc3ccccc3)cc2)nc1C
Reaction #73672
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(=O)c2ccc(Cc3ccccc3)cc2)sc1C(=O)NCCC#N
Reaction #73673
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #92008
solid
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(C(C)OC(=S)SC)c(OC)n2)c(OC)c1
Reaction #157836
O-[1-(6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-methoxypyridin-3-yl)ethyl] S-methyl carbonodithioate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(/C(=C/[C@H]2CCC(=O)N2Cc2ccc(OC)cc2OC)c2ccc(C(C)(C)C)cc2)nc1OC
Reaction #157837
(5R)-5-[(E)-2-(4-tert-butylphenyl)-2-(5-ethyl-6-methoxypyridin-2-yl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
Ausbeute 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(CCCCOS(C)(=O)=O)c(OC)n2)c(OC)c1
Reaction #157846
4-(6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-methoxypyridin-3-yl)butyl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(CCCCN(C)C)c(OC)n2)c(OC)c1
Reaction #157847
(5R)-5-[(E)-2-(4-tert-butylphenyl)-2-{5-[4-(dimethylamino)butyl]-6-methoxypyridin-2-yl}ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCN1C(=O)c2ccccc2C1=O)N1CCCC2=C1CCc1cc(Cl)ccc12
Reaction #173990
DOI: 10.1039/C8SC04228D
COC(=O)c1cnc(N2CCN(CCO)CC2)s1
Reaction #174651
DOI: 10.1039/C8SC04228D
Nc1nc2c(s1)CC(=O)CC2
Reaction #185330
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc(Cl)nc1C
Reaction #187218
DOI: 10.1039/C8SC04228D
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