部分構造検索

C=CCCCC=O

O=C(O)C(CCC(F)=C(F)F)C(=O)O
Reaction #6566
2-(3,4,4-Trifluoro-3-butenyl)malonic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12CCC(=O)C(Br)=C1c1ccc(OC)c(C)c1C2
Reaction #7946
4-bromo-9a-butyl-7-methoxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12Cc3cc(O)ccc3C1=C(C)C(=O)C(CCO)C2
Reaction #7967
(2RS,9aSR)-9a-butyl-7-hydroxy-2-(2-hydroxyethyl)-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12CCC(=O)C(CC)=C1c1cc(F)c(OC)c(C)c1C2
Reaction #7988
9a-butyl-4-ethyl-6-fluoro-7-methoxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12CCC(=O)C(CC)=C1c1cc(F)c(O)c(C)c1C2
Reaction #7989
9a-butyl-4-ethyl-6-fluoro-7-hydroxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CC1(CCI)CCC(=O)C(C)=C21
Reaction #7998
9a-(2-iodoethyl)-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(=O)C=CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44018
compound 103
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C(=CN(C)C)C(=O)C=CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44019
compound 104
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1c2cn[nH]c2C=CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44020
compound 105
収率 30.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(=O)CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44021
oil
収率 88.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)CCCC=C(c1ccc(CCNS(=O)(=O)c2ccc(Cl)cc2)cc1)c1cccnc1
Reaction #50406
6-(4-(2-(4-Chlorobenzenesulphonylamino)ethyl)phenyl)-6-(3-pyridyl)-hex-5-enoic acid diethylamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCc1ccc(C(=CCCCC(=O)O)c2cccnc2)cc1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #50407
6-(4-(2-(N-Methyl-4-chlorobenzenesulphonylamino)ethyl)phenyl)-6-(3-pyridyl)hex-5-enoic acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #50809
oil
DOI: 10.6084/m9.figshare.5104873.v1
CC[NH+](C(C)C)C(C)C
Reaction #52568
ethyldiisopropyl-ammonium
DOI: 10.6084/m9.figshare.5104873.v1
CC[NH+](CC)CC.O=C1C=C(O)C2CCC1C2
Reaction #52569
4-hydroxybicyclo[3.2.1]oct-3-en-2-one triethylammonium salt
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)C2=C(O)C3CCC(C3)C2=O)c([N+](=O)[O-])c1
Reaction #52570
4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)C2=C(O)C3CCC(C3)C2=O)c([N+](=O)[O-])c1
Reaction #52571
4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one
収率 44.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(F)(F)F)ccc1C(=O)OC1=CC(=O)C2CCC1C2
Reaction #52572
2-methyl-6-trifluoromethylnicotinic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)OC2=CC(=O)C3CCC2C3)c(Cl)c1Cl
Reaction #52573
2,3-Dichloro-4-methanesulfonylbenzoic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(CC(=O)OCC)C(=O)CCc2ccc(OCc3ccccc3)cc21
Reaction #54672
Ethyl-1-allyl-7-benzyloxy-2-oxo-1,2,3,4-tetrahydro-1-naphthaleneacetate
DOI: 10.6084/m9.figshare.5104873.v1
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