Substructure Search

4537

COC(=O)c1ccc(OC(=O)C2CCOCC2)cc1OC
Reaction #1770
methyl 4-(4-tetra-hydropyranoyloxy)-2-methoxy-benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC(=O)C2CCOCC2)ccc1C(=O)O
Reaction #1771
4-(4-tetrahydropyranoyloxy)-2-methoxy-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC(=O)C2CCc3ccccc32)ccc1C(=O)O
Reaction #1772
4-(1-indanoyloxy)-2-methoxy-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(OCC(F)(F)F)c(F)c1
Reaction #1800
4-trifluoroethoxy-5-fluorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)NC2CN3CCC2CC3)c(OC)c1.Cl
Reaction #3857
white solid
Yield 23.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(OC(N)=O)c1C/C=C(\C)CCC(=O)OCCN1CCOCC1)C(=O)OC2
Reaction #4600
morpholinoethyl E-6-(1,3-dihydro-4-carbamoyloxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C=O)c(OC(C)C)c1OC(C)C
Reaction #9404
aldehyde
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)O)c(OC(C)C)c1OC(C)C
Reaction #9405
alcohol
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(C=O)c(OC)cc2OC)c(OC)n1
Reaction #10745
5-(2,4-Dimethoxy-pyrimidin-5-yl)-2,4-dimethoxy-benzaldehyde
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(/C=C/C(=O)c3ccc(C(=O)O)cc3)c(OC)cc2OC)c(OC)n1
Reaction #10746
title compound
Yield 22.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2nccs2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10772
title compound
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cccn2C(=O)OC(C)(C)C)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10773
title compound
Yield 6.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cnn(C(=O)OC(C)(C)C)c2)cc1C=O
Reaction #10791
4-(5-formyl-2,4-dimethoxy-phenyl)-pyrazole-1-carboxylic acid tert-butyl ester
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cn[nH]c2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10792
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c2cn[nH]c(=O)c2c1
Reaction #58229
white solid
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(OCC[Si](C)(C)C)c1CC=O)C(=O)OC2
Reaction #61244
product
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(OCC[Si](C)(C)C)c1CC=C(C)C=O)C(=O)OC2
Reaction #61245
desired product
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(OCC[Si](C)(C)C)c1CC=C(C)CO)C(=O)OC2
Reaction #61246
product
Yield 97.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(OCC[Si](C)(C)C)c1CCO)C(=O)OC2
Reaction #61247
6-(2-Hydroxy-ethyl)-5-methoxy-4-methyl-7-(2-trimethylsilanyl-ethoxy)-3H-isobenzofuran-1-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(OCC[Si](C)(C)C)c1CCOCP(=O)(OC(C)C)OC(C)C)C(=O)OC2
Reaction #61248
desired product
DOI: 10.6084/m9.figshare.5104873.v1
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