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ClCCNCc1ccccc1

COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #1859
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)C(NC(=O)Cn1ccnc1)c1ccccc1CO2
Reaction #5136
product
DOI: 10.6084/m9.figshare.5104873.v1
CNCC(Cl)=C1CCN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2OC)CC1.O=C(O)C(F)(F)F
Reaction #43783
72
Ausbeute 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CNCC=C1CCN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2OC)CC1.O=C(O)C(F)(F)F
Reaction #43784
221
Ausbeute 15.0%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
Ausbeute 27.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1COCCN1Cc1ccccc1
Reaction #58598
oil
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63576
20.6
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=NS(=O)(=O)c1cc(C(C)(C)C)cc(CNC(=O)CCl)c1O
Reaction #63675
2-Chloro-N-[5-(1,1-dimethylethyl)-3-dimethylaminomethyleneaminosulfonyl-2-hydroxybenzyl]-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(CN)c(O)c(S(N)(=O)=O)c1.Cl
Reaction #63676
2-Aminomethyl-4-(1,1-dimethylethyl)-6-sulfamoylphenol hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N1Cc2ccccc2SC(Cl)C1
Reaction #64844
4-acryloyl-2-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine
Ausbeute 90.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N1Cc2ccccc2SC(OC/C=C(\C)CCC=C(C)C)C1
Reaction #64846
4-acryloyl-2-geranyloxy-2,3,4,5-tetrahydro-1,4-benzothiazepine
Ausbeute 68.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N1Cc2ccccc2SC(OC)C1
Reaction #64850
4-acryloyl-2-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #82192
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccccc1)C(=O)CCl
Reaction #85495
title compound
Ausbeute 63.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCOc1ccc(C(=O)OCC(=O)N(C)Cc2ccccc2)o1
Reaction #85496
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(CC2(O)CCN(C(=O)OC(C)(C)C)CC2)C(=O)C(Cl)c2ccccc2)cc1
Reaction #160223
tert-butyl 4-[[(2-chloro-2-phenyl-acetyl)-[(4-methoxyphenyl)methyl]amino]methyl]-4-hydroxy-piperidine-1-carboxylate
Ausbeute 73.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC3(CCN(C(=O)OC(C)(C)C)CC3)OC(c3ccccc3)C2=O)cc1
Reaction #160224
tert-butyl 10-[(4-methoxyphenyl)methyl]-9-oxo-8-phenyl-7-oxa-3,10-diazaspiro[5.5]undecane-3-carboxylate
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(N(Cc2ccccc2)C(=O)CCl)C(O)C1
Reaction #168295
tert-butyl 4-[benzyl(chloroacetyl)amino]-3-hydroxypiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@@H](N(Cc2ccccc2)C(=O)CI)[C@H](O)C1
Reaction #168296
trans-tert-butyl 4-[benzyl(iodoacetyl)amino]-3-hydroxypiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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