Busqueda de Subestructura

COC(=O)Cl

[N-]=[N+]=NCc1ccc(C(=N)NC(=O)OCc2ccccc2)cc1
Reaction #952
4-(benzyloxycarbonylamidino) benzyl azide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCCCC1
Reaction #1172
N-Cbz-piperidine
Rendimiento 59.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1282
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1414
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CCN(C(=O)OCc2ccccc2)N1
Reaction #1426
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@](O)(C(=O)OCCl)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1502
3-(Chloromethoxycarbonyl) Cholesterol
DOI: 10.6084/m9.figshare.5104873.v1
C#CCNC(=O)Nc1cc(NC(C)=O)c(F)cc1Cl
Reaction #1576
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)OCc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl
Reaction #1938
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](OC(=O)OCc3ccccc3)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #2079
3β-benzyloxycarbonyloxy-5-androsten-17-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@]23CCNC[C@@H]2CCC(=O)C3)c1.Cl
Reaction #2952
title compound
Rendimiento 70.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3430
oil
Rendimiento 44.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(Cc1cccs1)C(=O)O)OCc1ccccc1
Reaction #3768
N-(Benzyloxycarbonyl) β-thienyl-D,L-alanine
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2ccccc2N2CCCc3cc(Br)ccc32)CC1.O=C(O)/C=C\C(=O)O
Reaction #4137
product
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCCc3ccccc32)CC1
Reaction #4141
product
Rendimiento 61.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2ccccc2N2CCCc3ccccc32)CC1.O=C(O)/C=C\C(=O)O
Reaction #4143
product
Rendimiento 65.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2ccccc2N2CCCc3cc(Br)ccc32)CC1.O=C(O)/C=C\C(=O)O
Reaction #4195
product
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCCc3ccccc32)CC1
Reaction #4199
product
Rendimiento 61.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2ccccc2N2CCCc3ccccc32)CC1.O=C(O)/C=C\C(=O)O
Reaction #4201
product
Rendimiento 65.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(CCSc1ccc(F)cc1)C(=O)Oc1ccccc1
Reaction #4292
N-[2-[(4-Fluorophenyl)thio]ethyl]-N-(1-methylethyl)carbamic acid phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN1CC=CCC1)Oc1ccccc1
Reaction #4455
N-(phenoxy- carbonylamino)-1,2,3,6-tetrahydropyridine
Rendimiento 92.1%DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente