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1318282

CCOC(=O)C1CSCCN1
Reaction #1569
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cccc2c1N(C(=O)CBr)CCO2
Reaction #6460
4-bromoacetyl-5-benzoyl-3,4-dihydro-2H-1,4-benzoxazine
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OCc2ccccc2)cc1C(=O)COc1cccnc1
Reaction #6468
present title product
Ausbeute 25.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OCC(=O)c2cc(OCc3ccccc3)ccc2OC)c1
Reaction #6469
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC)N1CC(c2ccccc2)CCC1=O
Reaction #7495
ester
Ausbeute 70.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(Br)=N/Nc1ccccc1Cl
Reaction #7501
title compound
Ausbeute 71.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCNc1cc(Cl)cnc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11814
title compound
Ausbeute 36.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(C(=O)CCC(=O)c2ccccc2Cl)cc1
Reaction #43289
light yellow solid
Ausbeute 37.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)C(Br)c1ccccc1)c1ccccc1
Reaction #46637
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(C)(O)CC1)c1ccccc1
Reaction #46638
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(O)(c2ccccc2)CC1)c1ccccc1
Reaction #46643
title compound
Ausbeute 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC)Nc1ccc2ccccc2c1
Reaction #51328
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2cc(-c3cnc(NC4CCCCC4)s3)ccc12
Reaction #51635
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)C(Br)c1ccccc1
Reaction #54242
1-bromo-1-phenyl-3,3-dimethyl-butan-2-one
Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)C(Oc1ccc(Cl)cc1)c1ccccc1
Reaction #54243
1-phenyl-1-(4'-chlorophenoxy)-3,3-dimethyl-butan-2-one
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(C(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #54591
ethyl α-phthalimidopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(Cn1ccnc1)(OC)c1ccc2ccccc2c1
Reaction #54820
1-[2-(2-naphthyl)-2,2-dimethoxyethyl]imidazole
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CN1C(C)c1cccc2ccccc12
Reaction #57332
title compound
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1cccc2c1OCO2
Reaction #57545
1-benzo[1,3]dioxol-4-yl-2-bromo-ethanone
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1cccc2sccc12
Reaction #61845
1-benzo[b]thiophen-4-yl-2-bromo-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
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