Teilstruktursuche

CCC(C)C(=O)Cl

CCCC(Cc1ccccc1Br)C(=O)Cl
Reaction #1355
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1ccc([C@H]2CC[C@H](OC(=O)C3CCCCC3)CC2)cc1
Reaction #1751
trans-O-cyclohexanoyl-4-(4-dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)C1CC1C)c1nnc(C2CCCC2)[nH]c1=O
Reaction #7647
N-[1-(3-Cyclopentyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]-2-methylcyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)C1CC2C=CC1C2)c1nnc(C2CCCC2)[nH]c1=O
Reaction #7650
N-[1-(3-Cyclopentyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]bicyclo[2.2.1]hept-5-ene-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(CC)C(=O)NC(C)C(=O)O
Reaction #11353
2-(2-Ethyl)octanoylaminopropionic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc(C)c(C)c2n1CCC1CCN(C(=O)[C@@H]2C[C@H]2c2ccccc2)CC1
Reaction #11468
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(N)c2nc(C)n(CCCNC(=O)[C@@H]3C[C@H]3c3ccccc3)c2c1C
Reaction #11469
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CC[C@H](C(=O)c2ccccc2)CC1)OCc1ccccc1
Reaction #51225
N-benzyloxycarbonyl-trans-4-benzoylcylohexylamine
Ausbeute 77.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C(Cc1ccccc1)c1ccccc1
Reaction #51437
2,3-Diphenylpropionylchloride
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(N)(CCC(=O)O)C(=O)NC1C(=O)N2C(C(=O)O)=C(COC(C)=O)CSC12
Reaction #54311
7-[[2-amino-4-carboxy-2-vinylbutyryl]amino]-3-acetyloxymethyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccsc2C2CN(Cc3ccccc3)CCC12
Reaction #58553
subtitle compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccsc2C2CCN(Cc3ccccc3)CC12
Reaction #58557
subtitle compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccccc1)N1CC(C(=O)Cl)C(c2ccsc2)C1
Reaction #58565
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C(=O)Cl)CC1
Reaction #63547
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #63588
intermediate 17
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #63589
intermediate 18
DOI: 10.6084/m9.figshare.5104873.v1
CCSC(C#N)=C[C@@H]1[C@@H](C(=O)Cl)C1(C)C
Reaction #69882
(1R)-trans-3-[(1EZ)-2-cyano-2-(ethylthio)ethenyl]-2,2-dimethylcyclopropanecarboxylic acid chloride
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(=O)C2CC2c2ccccc2)sc1C(=O)NCc1ccccc1
Reaction #73609
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(N(C)S(=O)(=O)c2ccc(C)cc2)C(C)(C)C(=O)Cl)cc1
Reaction #93853
2,2-Dimethyl-4-(p-methoxyphenyl)-3-(N-methyl-p-toluenesulfonamido)butyryl chloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(=O)C(C)(C)C(N(C)S(=O)(=O)c1ccc(C)cc1)C2
Reaction #93854
3,4-Dihydro-2,2-dimethyl-7-methoxy-3-(N-methyl-p-toluenesulfonamido)-1(2H)-naphthalenone
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter