Substructure Search

383970

C=CCN(CC=C)C(=O)CCl
Reaction #3721
2-chloro-N,N-diallylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cccc(CC(C(C)=O)C(C)=O)c1
Reaction #4989
3-vinylbenzyl Acetylacetone
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3s2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10716
title compound
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3s2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10717
4-[3-(5-benzo[b]thiophen-2-yl-2,4-dimethoxy-phenyl)-E-acryloyl]-benzoic acid
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(=O)N(C)C)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10783
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(=O)N2CCOCC2)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10790
title compound
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3s2)cc1/C=C\C(=O)c1ccc(C(=O)O)cc1
Reaction #10800
title compound
Yield 21.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3s2)cc1/C=C/C(=O)c1ccc(C(=O)NCCN2CCOCC2)cc1
Reaction #10809
title compound
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3s2)cc1/C=C/C(=O)c1ccc(C(N)=O)cc1
Reaction #10812
title compound
Yield 94.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cccnc2)cc1/C=C/C(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #10823
title compound
Yield 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(=O)/C=C/c2cc(-c3cc4ccccc4s3)c(OC)cc2OC)cc1
Reaction #10842
title compound
Yield 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.COc1cc(OC)c(-c2cc3ccccc3s2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10844
4-[3E-(5-benzo[b]thien-2-yl-2,4-dimethoxy-phenyl)-acryloyl]-benzoic acid N-methyl-D-glucamine salt
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OCC=C(C)C=O
Reaction #50128
4-propionyloxy-2-methyl-2-buten-1-al
Yield 26.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(OC)CCC1C=O
Reaction #55738
methyl (5RS) 2-methoxy-5-formyl-1-cyclopentene-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(/CC(=O)OCC)c1ccccc1
Reaction #60215
diethyl (2Z)-3-phenylpent-2-ene-1,5-dioate
Yield 28.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC2=C(CSc3ccccc32)C1=O
Reaction #62612
brown crystalline solid
Yield 82.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(O)C(=O)C(C)O1
Reaction #64336
2,5-dimethyl-4-hydroxy-3[2H] furanone
Yield 81.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(O)C(=O)C(C)O1
Reaction #64337
2,5-dimethyl-4-hydroxy-3[2H] furanone
Yield 76.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(O)C(=O)C(C)O1
Reaction #64338
2,5-dimethyl-4-hydroxy-3[2H] furanone
Yield 74.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(CC(=O)OC)n1cc(-c2ncnc3c2ccn3COCC[Si](C)(C)C)cn1
Reaction #69217
dimethyl 3-[4-(7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]pentanedioate
Yield 64.0%DOI: 10.6084/m9.figshare.5104873.v1
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