Substructure Search

CCI

—
Reaction #2800
( 5 )
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccccc1CI
Reaction #2805
title compound
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccccc1CC(N=C(SC)SC)C(=O)N1C2CC3CCC2(CS1(=O)=O)C3(C)C
Reaction #2806
title compound
Yield 43.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2C[C@@H](C(N)=O)N(CCO)C2)cc1
Reaction #5206
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1CCO
Reaction #5210
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cccc2c(C3(CCCI)CCc4cc(F)ccc43)c[nH]c12
Reaction #41996
title compound
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCCC1(c2c[nH]c3c(NS(C)(=O)=O)cccc23)CCc2cc(F)ccc21
Reaction #41997
title compound
Yield 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cccc2c(C3(CCCN4CCOCC4)CCc4cc(F)ccc43)c[nH]c12
Reaction #41998
title compound
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCn1cc(-c2cnc3nnn(Cc4cc5cccnc5cc4F)c3n2)cn1
Reaction #44293
desired product
Yield 31.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CC(=O)CCc1ccc(OCc2ccccc2)cc1
Reaction #44324
6-(4-benzyloxyphenyl)-2,4-hexanedione
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
ICCOc1ccc(Cc2ccccc2)cc1
Reaction #44761
1-(2-iodoethoxy)-4-(benzyl)benzene
Yield 72.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN2CCCN(CCOc3ccc(Cc4ccccc4)cc3)CC2)cc1
Reaction #44794
methyl 4-[[hexahydro-4-[2-[4-(phenylmethyl)phenoxy]ethyl]-1H-1,4-diazepin-1-yl]methyl]benzoate
Yield 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](COCc1ccccc1)COC(CI)(c1ccccc1)c1ccccc1
Reaction #48672
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(c2ccccc2)(c2ccccc2)OC[C@@H]1COCc1ccccc1
Reaction #48673
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCCCC(C)(C)C(=O)OC
Reaction #50699
methyl 2,2-dimethyl-6-methoxycaproate
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(I)ccc(OC(C)=O)c1F
Reaction #52341
title compound
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC3CCOC3)cc2n1Cc1ccccc1
Reaction #68324
title compound
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC3CCOCC3)cc2n1Cc1ccccc1
Reaction #68407
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(I)C(=O)C2C3CCC(O3)C12
Reaction #69962
4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Yield 84.6%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(c2cnc(Cl)cc2C)C(=O)C2C3CCC(O3)C12
Reaction #69963
4-(6-chloro-4-methyl-pyridin-3-yl)-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Yield 64.9%DOI: 10.6084/m9.figshare.5104873.v1
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