Substructure Search

7064

CCOC(=O)C1(C(=O)OCC)Oc2ccccc2O1
Reaction #5674
1,3-benzodioxole-2,2-dicarboxylic acid, diethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/C=C/C(=O)OCC
Reaction #6708
ethyl sorbate
DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/C=C/C(=O)OCC
Reaction #9835
ethyl sorbate
DOI: 10.6084/m9.figshare.5104873.v1
C=C1[C@H](O[Si](C)(C)C(C)(C)C)CC(O)(CO)C[C@H]1O[Si](C)(C)C(C)(C)C
Reaction #10259
[(3R,5R)-3,5-Bis[(tert-butyldimethylsilyl)oxy]-1-hydroxy-4-methylenecyclohexyl]methanol
DOI: 10.6084/m9.figshare.5104873.v1
C=C1[C@H](O[Si](C)(C)C(C)(C)C)CC(O)(CO)C[C@H]1O[Si](C)(C)C(C)(C)C
Reaction #10260
diol
Yield 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C(=O)OCC)Oc2ccccc2O1
Reaction #10712
benzo[1,3]dioxole-2,2-dicarboxylic acid diethyl ester
Yield 73.2%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/C=C/C(=O)OCC
Reaction #47125
ethyl sorbate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(OCC)C(=O)N[C@@H]1C(=O)N(CCOCc2ccccc2)c2ccccc2-c2ccccc21
Reaction #59288
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(NC(=O)C1CC2CCCCC2N1C(=O)C(NC(=O)C(NC(=O)c1cnccn1)C1CCCCC1)C(C)(C)C)C(O)C(=O)OCC
Reaction #70196
32
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1O[C@H](CO)[C@@H]1O
Reaction #83112
desired product
Yield 96.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(OC)c1ccc(N)cc1
Reaction #84801
methyl 2-(4-aminophenyl)-2-methoxyacetate
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(OC)c1ccc(NS(=O)(=O)CCCCl)cc1
Reaction #84802
methyl 2-(4-(3-chloropropylsulfonamido)phenyl)-2-methoxyacetate
Yield 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC(Oc1ccc(C(=O)CCCCC)cc1)C(=O)OCC
Reaction #87310
Ethyl (RS)-2-[4-Hexanoylphenoxy]decanoate
Yield 80.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC(Oc1ccc(C(=O)CCCCC)cc1)C(=O)O
Reaction #87311
(RS)-2-[4-Hexanoylphenoxy]decanoic Acid
Yield 80.7%DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H](N)[C@@H](O)C(=O)OC
Reaction #92696
methyl (2R,3S)-3-amino-2-hydroxyhexanoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(OCc1ccccc1)C(=O)O
Reaction #93828
benzyloxymalonic acid
Yield 68.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1ccc(CCOc2ccc(OS(C)(=O)=O)cc2)cc1)OCC
Reaction #173458
DOI: 10.1039/C8SC04228D
COc1cc(CC(OC)C(=O)O)ccc1O
Reaction #173720
DOI: 10.1039/C8SC04228D
COC(=O)C(O)C(Oc1ccccc1)(c1ccccc1)c1ccccc1
Reaction #182025
DOI: 10.1039/C8SC04228D
COC(=O)C(O)C(C)(c1ccccc1)c1ccccc1
Reaction #183104
DOI: 10.1039/C8SC04228D
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