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O=C(Cl)CCc1ccccc1

CCC(Cc1ccccc1-c1ccccc1)C(=O)Cl
Reaction #1352
crude product
المردود 106.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(Cc1ccccc1Br)C(=O)Cl
Reaction #1355
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1Cc2c(Br)cccc2C1=O
Reaction #1358
4-bromo-2-i-butyl-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C(=O)Cl)Cc2ccccc21
Reaction #3493
3-methylindene-2-oyl chloride
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
Cc1cccc(C(=O)N(NC(=O)C2C=c3ccc4cccc5ccc(c3c54)C2=O)C(C)(C)C)c1
Reaction #49951
N'-t-butyl-N-pyrenonecarbonyl-N'-(3-toluoyl)hydrazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1cc(F)cc(F)c1)C(=O)Cl
Reaction #51499
t-butyl-(1S)-2-chloro-1-[3,5-difluorobenzyl]-2-oxoethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OC)c1-c1ccc(C[C@H](NC(=O)c2c(Cl)cccc2Cl)C(=O)Cl)cc1
Reaction #52958
N-(2,6-dichlorobenzoyl)-4-(2,6-dimethoxyphenyl)-L-phenylalanyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OC)c1-c1ccc(C[C@H](NC(=O)c2c(Cl)cccc2Cl)C(=O)NO)cc1
Reaction #52959
title compound
المردود 27.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(CC(=O)Cl)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #55185
3-(2',4'-difluoro-4-biphenylyl)butyryl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)CC(C)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #55186
3-(2',4'-difluoro-4-biphenylyl)butyric acid n-propyl ester
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)C(CC(=O)OCC#CCO)c1ccccc1
Reaction #56104
4-Hydroxy-2-butynyl 4-Cyano-3,4-diphenylbutyrate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1ccc2c(c1)CC(C(=O)NCCO)C2
Reaction #56202
N-(2'-hydroxyethyl) 5-benzoyl-indan-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(C)NC(C)=C(C(=O)Cl)C1c1cccc([N+](=O)[O-])c1
Reaction #62676
2,6-dimethyl-3-carbomethoxy-4-(3-nitrophenyl)-5-chlorocarbonyl-1,4-dihydropyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(=O)C2CC2c2ccccc2)sc1C(=O)NCc1ccccc1
Reaction #73609
title compound
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)CCc1cccc(F)c1
Reaction #84525
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C=C(/C)NC(=O)CCc1cccc(F)c1
Reaction #84526
title compound
المردود 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C1CC1c1cc(F)c(OCc2ccccc2)c(F)c1
Reaction #91180
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC[C@@H](Cc2ccccc2)N1C(=O)C1CC1c1cc(F)c(OCc2ccccc2)c(F)c1
Reaction #91181
title compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي