Busqueda de Subestructura

C1CCC(P(C2CCCCC2)C2CCCCC2)CC1

N#CC1=CC(=C2OCCO2)c2ccccc21
Reaction #10176
3-[1,3]dioxolan-2-ylidene-3H-indene-1-carbonitrile
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=CC(S(=O)(=O)c2ccccc2)c2ccccc21
Reaction #10177
3-benzenesulfonyl-3H-indene-1-carboxylic acid ethyl ester
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C1CCC([PH+](C2CCCCC2)C2CCCCC2)CC1.c1ccc([B-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #42144
tricyclohexylphosphonium tetraphenylborate
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCc1ccccc1
Reaction #42152
1-phenylheptane
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCc1ccccc1
Reaction #42170
1-phenylheptane
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #42664
title compound
Rendimiento 57.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc2c1C(=O)N=C(NC(=O)OC(C)(C)C)NCc1cc(Cl)c(c(Cl)c1)NC(=O)CN(C(=O)OC(C)(C)C)CC=CCOc1ccc-2cc1
Reaction #42684
crude product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc2c1C(=O)N=C(NC(=O)OC(C)(C)C)NCc1cc(Cl)c(c(Cl)c1)NC(=O)CN(C(=O)OC(C)(C)C)CCCC=CCOc1ccc-2cc1
Reaction #42686
crude product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1snc2c1C(=O)N=C(NC(=O)OC(C)(C)C)NCc1cc(Cl)c(c(Cl)c1)NC(=O)CN(C(=O)OC(C)(C)C)CCCC=CCOc1ccc-2cc1
Reaction #42687
crude product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc2c1C(=O)N=C(NC(=O)OC(C)(C)C)NCc1cc(Cl)c(c(Cl)c1)NC(=O)CN(C(=O)OC(C)(C)C)CCCC/C=C/COc1ccc-2cc1
Reaction #42690
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC=C[C@H]2CC[C@@H](c3cc(F)c(F)c(F)c3)N12
Reaction #44615
title compound
Rendimiento 70.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC=C[C@H]2COC[C@@H](c3cc(F)c(F)c(F)c3)N12
Reaction #44627
title compound
Rendimiento 26.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC=C[C@H]2CCC[C@@H](c3ccc(Cl)cc3)N12
Reaction #44643
title compound
Rendimiento 222.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(C2CC=CC2)c2oc(C3CC3)nc2c1C#N
Reaction #45867
compound
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C12CC1C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(O[Si](C)(C)C(C)(C)C)CC1C(=O)N2
Reaction #46089
14-tert-butoxycarbonylamino-18-(tert-butyl-dimethyl-silanyloxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid ethyl ester
Rendimiento 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@@H](CC2CC=CCO2)COC1(C)C
Reaction #47307
(S)-4-(3,6-dihydro-2H-pyran-2-ylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid t-butyl ester
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](CC(C)C)N1CC(Oc2cccc(C3CC3)c2F)=CC1=O
Reaction #47445
(S)-2-[4-(3-cyclopropyl-2-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid ethyl ester
Rendimiento 710.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)c(C2CC2)c1
Reaction #48069
3-cyclopropyl-4-fluorophenylamine
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(Cl)cc(C(=O)N(CCc2cc(F)cc(C(F)(F)F)c2)Cc2ccc(C(C)(C)C)cc2)c1
Reaction #48089
yellow solid
Rendimiento 61.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(CC1(O)CC=CC1)OC
Reaction #48279
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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