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19096

COc1cc(OC)c(-c2cccs2)cc1C=O
Reaction #10719
2,4-dimethoxy-5-thiophen-2-yl-benzaldehyde
Ausbeute 94.0%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
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cccs2)cc1/C=C/C(=O)c1ccccc1C(=O)O
Reaction #10741
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cccs2)cc1/C=C/C(=O)c1cccc(C(=O)O)c1
Reaction #10753
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(OC)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10770
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cccs2)cc1/C=C/C(=O)c1ccc(C(C)(C)C(=O)O)cc1
Reaction #10798
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCc2nnn[nH]2)c(C=O)cc1-c1cccs1
Reaction #10807
4-methoxy-2-(1H-tetrazol-5-ylmethoxy)-5-thiophen-2-yl-benzaldehyde
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCc2nnn[nH]2)c(/C=C/C(=O)c2ccc(S(N)(=O)=O)cc2)cc1-c1cccs1
Reaction #10808
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCc2nc3ccccc3[nH]2)c(/C=C/C(=O)c2ccc(S(N)(=O)=O)cc2)cc1-c1cccs1
Reaction #10836
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCc2ccccn2)c(/C=C/C(=O)c2ccc(S(N)(=O)=O)cc2)cc1-c1cccs1
Reaction #10837
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCn2nnc3ccccc32)c(/C=C/C(=O)c2ccc(S(N)(=O)=O)cc2)cc1-c1cccs1
Reaction #10838
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C=O)c(Cl)cc1OCc1nc2ccccc2[nH]1
Reaction #183704
DOI: 10.1039/C8SC04228D
COc1cc(OC)c(-c2cccs2)cc1C=O
Reaction #271752
DOI: 10.1039/C8SC04228D
COc1cc(C=O)c(Cl)cc1OCc1nc2ccccc2[nH]1
Reaction #340637
4-(1H-benzoimidazol-2-ylmethoxy)-2-chloro-5-methoxy-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(O)c2c[nH]c3ncc(Cl)cc23)c(Cl)cc1OCc1nc2ccccc2[nH]1
Reaction #340638
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C=O)c(F)cc1OCc1nc2ccccc2[nH]1
Reaction #340642
desired compound
Ausbeute 45.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C=O)c(F)cc1OCc1nc2ccccc2n1C
Reaction #340643
desired compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(COc2cc(F)c(C=O)cc2OC)nc2ccccc21
Reaction #340657
desired compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cccs2)cc1C=CC(=O)c1cccc(C(=O)O)c1
Reaction #390110
DOI: 10.1039/C8SC04228D
COc1cc(OC)c(-c2cccs2)cc1C=O
Reaction #434514
2,4-dimethoxy-5-thien-2-ylbenzaldehyde
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
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