بحث البنية الفرعية

3017

C[C@@H](OC(=O)c1ccc([N+](=O)[O-])cc1)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44602
title compound
المردود 76.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44603
title compound
المردود 95.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](OC(=O)c1ccc([N+](=O)[O-])cc1)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44633
title compound
المردود 76.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44634
title compound
المردود 95.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1c2ccccc2CN1C(=O)OC(C)(C)C
Reaction #52158
N-BOC-1,3-dihydro-2H-isoindol-1-carboxylic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)c2ccccc2CN1C(=O)OC(C)(C)C
Reaction #52159
N-BOC-1-methyl-1,3-dihydro-2H-isoindol-1-carboxylic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)c1ccc(C(NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #61088
tert-butoxycarbonylamino-[4-(diethoxy-phosphoryl)-phenyl]-acetic acid benzyl ester
المردود 93.1%DOI: 10.6084/m9.figshare.5104873.v1
COCO[C@@H]1C(Br)c2ccccc2[C@H]1N(COC)C(=O)OC(C)(C)C
Reaction #92712
tert-butyl[(1R,2S)-3-bromo-2-(methoxymethoxy)-2,3-dihydro-1H-inden-1-yl](methoxymethyl)carbamate
المردود 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](c1ccccc1)[C@@H](CO[Si](C)(C)C(C)(C)C)OC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #92713
(6S,7R)-2,2,3,3,11,11-hexamethyl-9-oxo-7-phenyl-4,10-dioxa-8-aza-3-siladodecan-6-yl 4-nitrobenzoate
المردود 65.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NC(C(=O)O[C@H]1CN2CCC1CC2)c1ccccc1
Reaction #164158
(R)-quinuclidin-3-yl 2-amino-2-phenylacetate di-hydrochloride
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(S(=O)(=O)c2ccc(-c3cnc(N)c(-c4nnc(-c5ccc(C6COCCN6C(=O)OC(C)(C)C)cc5)o4)n3)cc2)C1
Reaction #165906
sub-title product
المردود 51.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COCC(NC(=O)OC(C)(C)C)(c1cccc(Br)c1)C(F)(F)F
Reaction #168733
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COCC(N)(c1cccc(Br)c1)C(F)(F)F
Reaction #168734
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(c2ccc(NC(=O)c3ccc(Cl)cc3)cc2)COC1(C)C
Reaction #179948
DOI: 10.1039/C8SC04228D
CCOP(=O)(OCC)c1ccc(C(NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #180105
DOI: 10.1039/C8SC04228D
NC(CO)c1ccc(NC(=O)Nc2ccc(Cl)cc2)cc1
Reaction #184827
DOI: 10.1039/C8SC04228D
CCC1(CC)OC(C(=O)O)C(c2ccccc2)N1C(=O)OC(C)(C)C
Reaction #193103
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(C(=O)OCC(=O)c1ccccc1)c1ccc(O)cc1
Reaction #196457
DOI: 10.1039/C8SC04228D
COC(=O)C(NC(=O)OC(C)(C)C)c1ccc(-c2c(OC)cccc2OC)cc1
Reaction #206152
DOI: 10.1039/C8SC04228D
CCC(CC)(c1ccc(CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C)c(C)c1)c1ccc(-c2ccc(C(NC(=O)OC(C)(C)C)C(=O)OC)cc2)c(C)c1
Reaction #213210
DOI: 10.1039/C8SC04228D
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