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96109

COC(=O)[C@@H]1C[C@H](NS(=O)(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40606
43
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2c1OC1C3CCC4(C(=O)N(CC5CC5)CCC214)C(COCC=Cc1ccccc1)C3
Reaction #63806
5-cinnamyloxymethyl-3-cyclopropylmethyl-9-methoxy-1,2,5,6,7,7a-hexahydro-4a,7-ethanobenzofuro[3,2-e]isoquinolin-4(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66028
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66029
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66030
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCC(c2ccc(-c3cnc(Nc4cccc(F)c4)nc3)cc2)CC1
Reaction #163208
(4-{4-[2-(3-Fluorophenylamino)-pyrimidin-5-yl]-phenyl}-cyclohexyl)-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1CCC(c2ccc(-c3cnc(Nc4cccc(F)c4)nc3)cc2)CC1
Reaction #163209
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCC(c2ccc(-c3cnc(Cl)nc3)cc2)CC1
Reaction #163210
{4-[4-(2-chloro-pyrimidin-5-yl)-phenyl]-cyclohexyl}-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1CCC(c2ccc(-c3cnc(Nc4ccc(C(F)(F)F)nc4)nc3)cc2)CC1
Reaction #163211
(4-{4-[2-(6-Trifluoromethyl-pyridin-3-ylamino)-pyrimidin-5-yl]-phenyl}-cyclohexyl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CCC(c2ccc(C(=O)CBr)cc2)CC1
Reaction #163212
title compound
Ausbeute 85.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CCC(c2ccc(-c3csc(Nc4cccc(OC)c4)n3)cc2)CC1
Reaction #163213
(4-{4-[2-(3-Methoxyphenylamino)-thiazol-4-yl]-phenyl}-cyclohexyl)-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1CCC(c2ccc(-c3csc(Nc4cccc(F)c4)n3)cc2)CC1
Reaction #163215
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CCC(c2ccc(C(=O)CN=[N+]=[N-])cc2)CC1
Reaction #163216
title compound
Ausbeute 103.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CCC(c2ccc(-c3cnc(Nc4cccc(Cl)c4)o3)cc2)CC1
Reaction #163217
title compound
Ausbeute 63.8%DOI: 10.6084/m9.figshare.5104873.v1
O=CCC1CCC(c2ccc(-c3cnc(Nc4cccc(Cl)c4)o3)cc2)CC1
Reaction #163218
title compound
Ausbeute 56.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCC(c2ccc(-c3ccc(Nc4ccc(C(F)(F)F)nc4C)nc3)cc2)CC1
Reaction #163228
compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(F)(F)F)ccc1Nc1ccc(-c2ccc(C3CCC(CC(=O)O)CC3)cc2)cn1
Reaction #163229
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCC(c2ccc(-c3ccc(Br)cn3)cc2)CC1
Reaction #163236
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCC(c2ccc(-c3ccc(Nc4ccc(C(F)(F)F)nc4)cn3)cc2)CC1
Reaction #163237
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1CCC(c2ccc(-c3ccc(Nc4ccc(C(F)(F)F)nc4)cn3)cc2)CC1
Reaction #163238
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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