Substructure Search

5911

O=c1cc(O)c2ccc(OCc3ccccc3)cc2o1
Reaction #1815
7-Benzyloxy-4-hydroxy-coumarin
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(O)c2ccc(O)cc2o1
Reaction #1816
4,7-Dihydroxy-coumarin
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=C1C(=O)Oc2cc(OCc3ccccc3)ccc2C1=O
Reaction #1817
3-diazo-4-oxo-7-benzyloxy-3,4-dihydrocoumarin
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(O)c2ccc(OCc3ccccc3)cc2o1
Reaction #1818
7-Benzyloxy-4-hydroxy-coumarin
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(O)c2ccc(O)cc2o1
Reaction #1819
4,7-Dihydroxy-coumarin
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=C1C(=O)Oc2cc(OCc3ccccc3)ccc2C1=O
Reaction #1820
3-diazo-4-oxo-7-benzyloxy-3,4-dihydrocoumarin
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O)ccc2c(O)c(C(=O)Nc3cccc(F)c3)c(=O)oc12
Reaction #83610
title product
Yield 27.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCc2ccccc2)ccc2c(O)c(C(=O)Nc3cccc(Br)c3)c(=O)oc12
Reaction #83612
title compound
Yield 15.2%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(O)c2ccc(O)cc2o1
Reaction #1319467
DOI: 10.1039/C8SC04228D
Cc1c(OCc2ccccc2)ccc2c(O)c(C(=O)Nc3cccc(Br)c3)c(=O)oc12
Reaction #1690211
title compound
Yield 15.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)c1c(O)c2ccc(OCc3ccccc3)cc2oc1=O)C(=O)O
Reaction #2278122
2-(S)-[(7-Benzyloxy-4-hydroxy-2-oxo-2H-chromene-3-carbonyl)-amino]-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1