Recherche de Sous-structure

2605

CCOP(=O)(OCC)C(CCC#N)S(=O)(=O)[O-].[Li+]
Reaction #2791
3-cyano-1-diethoxyphosphinylpropanesulfonic acid lithium salt
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(=O)[O-].[Li+]
Reaction #4035
Lithium heptanoate
Rendement 51.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)C(=O)[O-].[Li+]
Reaction #4967
lithium hydroxystearate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC(C)(C)C(=O)O)c(-c2cccs2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10764
title compound
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O)c(-c2cccs2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10771
title compound
Rendement 5.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10774
title compound
Rendement 15.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC(C)(C)C(=O)O)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10775
title compound
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCCN2CCOCC2)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1.Cl
Reaction #10776
title compound
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(CO)CO)c(/C=C/C(=O)c2ccc(S(N)(=O)=O)cc2)cc1-c1cccs1
Reaction #10805
title compound
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCCN2CCOCC2)c(/C=C/C(=O)c2ccc(C(N)=O)cc2)cc1-c1cccs1
Reaction #10811
title compound
Rendement 57.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC(C)(C)C(=O)O)c(-c2cccs2)cc1/C=C/C(=O)c1ccc(NS(C)(=O)=O)cc1
Reaction #10817
title compound
Rendement 15.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC(C)(C)C(=O)O)c(-c2cccs2)cc1/C=C/C(=O)c1ccc(N(C)S(C)(=O)=O)cc1
Reaction #10819
2-(4-{3-[4-(Methanesulfonyl-methyl-amino)-phenyl]-3-oxo-E-propenyl}-5-methoxy-2-thiophen-2-yl-phenoxy)-2-methyl-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2nncn2CC(C)C)cc1/C=C/C(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #10832
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2nncn2CC(C)C)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10833
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2c[nH]c(C3CC3)n2)cc1/C=C/C(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #10834
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(C2C=CCO2)cc1/C=C/C(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #10846
title compound
Rendement 72.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Oc2cccc(C)n2)c(/C=C/C(=O)c2ccc(S(N)(=O)=O)cc2)cc1-c1cccs1
Reaction #10848
title compound
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(Oc1ccccc1)c1ccc(OC)cc1
Reaction #42710
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)[O-])N1CC(Oc2cccc(N3CCCC3)c2F)=CC1=O.[Li+]
Reaction #47436
(S)-2-[4-(2-fluoro-3-pyrrolidin-1-yl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid lithium salt
Rendement 126.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC[C@H](C(=O)OC(C)(C)C)[C@H](O)COC(C)=O
Reaction #48321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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