Substructure Search

18630

COc1cc(OC)c(-c2cc3ccccc3s2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10717
4-[3-(5-benzo[b]thiophen-2-yl-2,4-dimethoxy-phenyl)-E-acryloyl]-benzoic acid
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cccs2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10720
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3s2)cc1/C=C/C(=O)c1ccc(Nc2c(N)c(=O)c2=O)cc1
Reaction #10821
title compound
Yield 5.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C1SC=CN1C(=O)OCC
Reaction #305411
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2snc(Cc3ccc([N+](=O)[O-])cc3)c12
Reaction #314815
desired product
Yield 47.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1CCC(=O)c1cccc(C=Cc2ccc3ccc(Cl)cc3n2)c1
Reaction #336222
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1CCC(=O)c1cccc(C=Cc2ccc3ccc(Cl)cc3n2)c1
Reaction #336227
title compound
Yield 92.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1ccccc1OCc1ccccc1
Reaction #409202
title product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)c1ccccc1CCC(=O)c1cccc(C=Cc2ccc3ccc(Cl)cc3n2)c1
Reaction #414103
foam
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)OCC[Si](C)(C)C)c1ccccc1CCC(=O)c1cccc(C=Cc2ccc3ccc(Cl)cc3n2)c1
Reaction #414109
title compound
Yield 83.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1CCC(=O)c1cccc(C=Cc2ccc3ccc(Cl)cc3n2)c1
Reaction #414112
title compound
Yield 92.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)c1ccccc1CCC(=O)c1cccc(C=Cc2ccc3ccc(Cl)cc3n2)c1
Reaction #429183
foam
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)OCC[Si](C)(C)C)c1ccccc1CCC(=O)c1cccc(C=Cc2ccc3ccc(Cl)cc3n2)c1
Reaction #429189
title compound
Yield 83.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1CCC(=O)c1cccc(C=Cc2ccc3ccc(Cl)cc3n2)c1
Reaction #429192
title compound
Yield 92.2%DOI: 10.6084/m9.figshare.5104873.v1
[Li][O]Cc1ccccc1
Reaction #442720
benzyloxy lithium
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2c(c1)C=C(Br)CO2
Reaction #489296
3-bromo-6-chloro-2H-chromene
Yield 27.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Cl)nc1)N1CCCNCC1
Reaction #491727
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2ccc3c(c2)CCOC3)C(=O)O1
Reaction #575549
title compound
Yield 50.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2ccc3c(c2)CCSC3)C(=O)O1
Reaction #575551
title compound
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC[C@H]1CN(c2ccc3c(c2)CN(C(=O)OCc2ccccc2)CC3)C(=O)O1
Reaction #575558
title compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
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