بحث البنية الفرعية

CCOC(C)(OCC)OCC

CCOC(=O)CC(C)(C)C=CC(Cl)(Cl)C(F)(F)F
Reaction #1343
ethyl 6,6-dichloro-3,3-dimethyl-7,7,7-trifluorohept-4-enoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@H](O)[C@@H](OC(=O)c2ccccc2)[C@H](O[C@@H]2[C@H](O[C@@H]3O[C@@H](C)[C@@H](OCc4ccccc4)[C@@H](OCc4ccccc4)[C@@H]3OCc3ccccc3)[C@@H](OC(=O)c3ccccc3)[C@H](OCC[Si](C)(C)C)O[C@@H]2COC(=O)c2ccccc2)O[C@@H]1COC(=O)c1ccccc1
Reaction #2722
title compound 11a
المردود 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(C)(C)C=CC(Cl)(Cl)C(F)(F)F
Reaction #3112
ethyl 6,6-dichloro-3,3-dimethyl-7,7,7-trifluorohept-4-enoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CCl)(OCC)OCC
Reaction #4016
2-chloro-1,1,1-triethoxyethane
المردود 77.1%DOI: 10.6084/m9.figshare.5104873.v1
ClCc1nc2ccccc2s1
Reaction #4017
2-chloromethylbenzothiazole
المردود 91.3%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc2sc(CCl)nc2c1
Reaction #4018
2-Chloromethyl-5-trifluoromethylbenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
ClCc1nc2ncccc2o1
Reaction #4019
2-Chloromethyl-oxazolo[4,5-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
ClCc1nc2cccnc2s1
Reaction #4020
2-Chloromethylthiazolo[5,4-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
ClCc1nc2cc(Br)ccc2o1
Reaction #4021
2-Chloromethyl-5-bromobenzoxazole
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cnc3cc(Br)ccc3c2n1CC(C)(C)O
Reaction #9480
1-(7-bromo-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol
المردود 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cnc3cc(Br)ccc3c2n1CC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #9537
tert-butyl 4-[(7-bromo-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]piperidine-1-carboxylate
المردود 77.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(Oc2ccccc2)c2nc(C)n(CCNC(=O)OC(C)(C)C)c2c1C
Reaction #11464
tert-butyl 2-(2,6,7-trimethyl-4-phenoxy-1H-imidazo[4,5-c]pyridin-1-yl)ethylcarbamate
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1C[C@H](N)[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@H](O)[C@@H]3O[C@@]4(O[C@@H]23)O[C@H]([C@H](N)CO)[C@H](O)[C@H](O)[C@H]4O)[C@H]1O
Reaction #42643
hygromycin
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc2c(C#N)c(C)c(Br)c(F)c2o1
Reaction #45670
compound
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C#C[Si](C)(C)C)(OCC)OCC
Reaction #52306
title compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(OCC)(OCC)OCC
Reaction #52307
title compound
المردود 55.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C#Cc1cncc(S(C)(=O)=O)c1)(OCC)OCC
Reaction #52309
title compound
المردود 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C#Cc1cncc(S(C)(=O)=O)c1
Reaction #52310
title compound
المردود 58.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C#Cc1cncc(OCC(F)(F)F)c1)(OCC)OCC
Reaction #52329
title compound
المردود 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cncc(C#CC(OCC)(OCC)OCC)c1
Reaction #52331
title compound
المردود 37.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي