Busqueda de Subestructura

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COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OC5CCS(=O)(=O)CC5)cc4C)c3)ccc21
Reaction #43943
title compound
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)c(C)c(OCCCS(C)(=O)=O)c(C)c4C)c3)ccc21
Reaction #43946
title compound
Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)cc4C)c3)ccc21
Reaction #43948
title compound
Rendimiento 82.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)c(F)c4C)c3)ccc21
Reaction #43951
title compound
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)c(Cl)c(OCCCS(C)(=O)=O)c(Cl)c4C)c3)ccc21
Reaction #43960
title compound
Rendimiento 89.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(OCCCS(C)(=O)=O)cc(CC)c1-c1cccc(COc2ccc3c(c2)OC[C@H]3CC(=O)OC)c1
Reaction #43962
title compound
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\C)OCC1COc2ccccc2O1
Reaction #47270
(E)-3-(2,3-dihydro-benzo[1,4]dioxin-2-ylmethoxy)-but-2-enoic acid ethyl ester
Rendimiento 40.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(F)ccc2n1CCc1cccnc1
Reaction #48019
expected product
Rendimiento 41.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(C(F)(F)F)ccc2n1Cc1ccncc1
Reaction #48021
expected product
Rendimiento 77.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO1
Reaction #48633
desired compound
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](COC2CCCCC2)OC[C@@H]1[C@@H](OCc1ccccc1)[C@H](Cc1cc(F)cc(F)c1)N(Cc1ccccc1)Cc1ccccc1
Reaction #48659
desired compound
Rendimiento 84.7%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52150
cyclic peptides
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Cc1ccccc1)Cc1cc2cc(OCCCNc3ccccn3)ccc2[nH]1
Reaction #52257
title compound
Rendimiento 38.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1cc2cc(OCCCNc3ccccn3)ccc2[nH]1)C(=O)O
Reaction #52258
title compound
Rendimiento 15.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(Cc1cc2cc(OCCCNc3ccccn3)ccc2[nH]1)C(=O)O
Reaction #52260
title compound
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52263
solid
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(N)P(O)O
Reaction #54255
1-amino-n-heptanephosphonous acid
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccccc1OCCCc1ccc(Br)cc1
Reaction #61307
3-(4Bromophenyl)prop-1-yl 2-chlorophenyl ether
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(C)c(OCCc2ccc(Br)cc2)c1
Reaction #61308
title compound
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(Cc2ccoc2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #61711
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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