부분 구조 검색

CCC1CO1

COc1ccc(C2C(=O)CCc3ccccc32)cc1
Reaction #41960
1-(4-methoxyphenyl)-3,4-dihydro-1H-naphthalene-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCC(=O)C2c1ccccc1
Reaction #41962
6-methoxy-1-phenyl-3,4-dihydro-1H-naphthalene-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC2(O1)C(C)(C)CCCC2(C)O
Reaction #74885
2,6,10,10-tetramethyl-1-oxa-spiro[4.5]dec-3-ene-6-ol
수율 174.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#C/C=C/C23OC2(C)CCCC3(C)C)nc1
Reaction #81518
Ethyl (±)-6-[(3E)-4-(1,2-Epoxy-2,6,6-trimethylcyclohexanyl)but-3-en-1-ynyl)nicotinate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)CN1CCOCC1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](Cc1ccccc1)C(=O)[C@@]1(C)CO1
Reaction #87187
(S)-3-cyclopropyl-N-((S)-1-((R)-2-methyloxiran-2-yl)-1-oxo-3-phenylpropan-2-yl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanamide
수율 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)[C@H]2CCCO2)C(=O)N[C@@H](Cc2ccccc2)C(=O)[C@@]2(C)CO2)cc1
Reaction #87206
(R)-N-((S)-1-(((S)-3-(4-methoxyphenyl)-1-(((S)-1-((R)-2-methyloxiran-2-yl)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxopropan-2-yl)amino)-1-oxopropan-2-yl)tetrahydrofuran-2-carboxamide
수율 57.2%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2(C(F)(F)c3ccc(Oc4ccc(C(F)(F)F)cn4)cn3)CO2)c(F)c1
Reaction #91534
title compound
수율 78.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2(C(F)(F)c3ccc(Oc4ccc(Cl)cn4)cn3)CO2)c(F)c1
Reaction #91535
title compound
수율 16.6%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Oc2ccc(C(F)(F)C3(c4ccc(F)cc4F)CO3)nc2)nc1
Reaction #91536
title compound
수율 99.5%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2(C(F)(F)c3ccc(OCC(F)(F)F)cn3)CO2)c(F)c1
Reaction #91537
2-((2-(2,4-difluorophenyl)oxiran-2-yl)difluoromethyl)-5-(2,2,2-trifluoroethoxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2(C(F)(F)c3ccc(OC4CC4(F)F)cn3)CO2)c(F)c1
Reaction #91538
title compound
수율 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c2cc(C3CC3)c(N(CCCC3CO3)S(C)(=O)=O)cc2nn1-c1ccc(Cl)cc1
Reaction #91817
( ii )
수율 118.7%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c2cc(C3CC3)c(N(CCCC3CCO3)S(C)(=O)=O)cc2nn1-c1ccc(Cl)cc1
Reaction #91818
Compound ( 4 )
수율 16.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C(Cc1ccccc1)C1CO1
Reaction #180606
DOI: 10.1039/C8SC04228D
CC1C=CC2(O1)C(C)(C)CCCC2(C)O
Reaction #184137
DOI: 10.1039/C8SC04228D
CCOC(C)OC1CCC(C)(OC)C(OC(C)=O)C=CC(C)C(C(C)=CC=CC(C)(CC2OC2C(C)C(CC)OC(C)OCC)OC(C)OCC)OC(=O)C1
Reaction #185552
DOI: 10.1039/C8SC04228D
COC1C(OC(=O)NC2CCCCC2)CCC2(CO2)C1C1(C)OC1CC=O
Reaction #198844
DOI: 10.1039/C8SC04228D
CCOC(C)OC1(C)CCC(O[Si](CC)(CC)CC)CC(=O)OC(C(C)=CC=CC(C)CC2OC2C(C)C(CC)OC(=O)c2ccccc2)C(C)C=CC1O
Reaction #204819
DOI: 10.1039/C8SC04228D
CC(n1ccn(-c2ccc(-n3cnnn3)cc2)c1=O)C1(c2ccccc2F)CO1
Reaction #208056
DOI: 10.1039/C8SC04228D
O=C(c1ccc(F)c(F)c1Nc1ccc(I)cc1F)N1CC2(C1)OC2CC1OCCO1
Reaction #208701
DOI: 10.1039/C8SC04228D
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