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10985

O=C(C1CC1)N1CCC(CO)CC1
Reaction #5234
liquid
Ausbeute 63.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2CCCC(OCCO)c3cc(Cl)ccc32)cc1
Reaction #5684
5-(2-hydroxyethoxy)-7-chloro-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](CO)CCCO)OCc1ccccc1
Reaction #7382
title compound
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc(C2CC2)cc1
Reaction #7456
4-cyclopropylbenzyl alcohol
Ausbeute 95.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7713
desired product
DOI: 10.6084/m9.figshare.5104873.v1
OCc1cccc(-c2nn3c(c2-c2ccnc4ccccc24)CCC3)n1
Reaction #8370
title compound
Ausbeute 58.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(CO)(CCO[Si](C)(C)C(C)(C)C)CC1
Reaction #8863
tert-Butyl 4-hydroxymethyl-4-(2-(tert-butyldimethylsilyloxy)eth-1-yl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(CO)CCC1
Reaction #9327
1-3
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #9382
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CC[C@@H](CCO)N1C(=O)OC(C)(C)C
Reaction #10516
di-tert-butyl (2S,5S)-5-hydroxyethylpyrrolidine-1,2-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc(Nc2nc(-c3ccccc3)nc3ccccc23)[nH]n1
Reaction #11923
(5-Hydroxymethyl-2H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1ccc(F)c(F)c1)NCC(O)c1cc(O)cc2c1OCC(=O)N2
Reaction #40396
8-{2-[2-(3,4-difluorophenyl)-1,1-dimethylethylamino]-1-hydroxyethyl}-6-hydroxy-4H-benzo [1,4]oxazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1ccc(F)cc1Cl)NCC(O)c1cc(O)cc2c1OCC(=O)N2
Reaction #40397
8-{2-[2-(2-chloro-4-fluorophenyl)-1,1-dimethylethylamino]-1-hydroxyethyl}-6-hydroxy-4H-benzo[1,4]oxazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(CO)cc2cccc(Br)c21
Reaction #40903
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)cc(CO)c1
Reaction #42379
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)Cc1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42397
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC2(CC(CO)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44023
mixture
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Cl)cc1)N1[C@H](CO)Cc2[nH]ncc2[C@@H]1CO
Reaction #44042
cis-(5-(4-Chlorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine-4,6-diyl)dimethanol
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCCN1c1cccc(CCO)c1
Reaction #44095
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Cl)cn1)c1oc2ccc(CO)nc2c1NC(=O)[C@H]1CC[C@H](N2CCOCC2=O)CC1
Reaction #44963
title compound
Ausbeute 28.1%DOI: 10.6084/m9.figshare.5104873.v1
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