Поиск подструктуры

852892

COC(=O)[C@@H]1CC[C@H]2CC(NC(=O)OCc3ccccc3)C(=O)N21
Reaction #10520
methyl (3S,7aS)-6-benzyloxycarbonylamino-5-oxohexahydropyrrolizine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](C[N+](=O)[O-])c1cccc(F)c1F)C(=O)OCc1ccccc1
Reaction #42668
title compound
Выход 87.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](CN)c1cccc(F)c1F)C(=O)O
Reaction #42669
title compound
Выход 97.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN(C(=O)OC(C)(C)C)c1ccc(Br)cn1
Reaction #46528
title compound
Выход 52.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CNc1ccc(Br)cn1
Reaction #46529
title compound
Выход 100.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CCC(CN)c1cccc(Cl)c1Cl)C(=O)OCc1ccccc1
Reaction #48399
title compound
Выход 182.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](C[N+](=O)[O-])c1cccc(F)c1F)C(=O)OCc1ccccc1
Reaction #48412
title compound
Выход 87.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](CN)c1cccc(F)c1F)C(=O)O
Reaction #48413
title compound
Выход 97.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@@H](c1cccc(F)c1F)C(CO)[N+](=O)[O-])C(=O)OCc1ccccc1
Reaction #48447
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@@H](c1cccc(F)c1F)C(N)CO)C(=O)O
Reaction #48448
title compound
Выход 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(CO)C1CCCCC1
Reaction #56778
tert-butyl 1-cyclohexyl-2-hydroxyethylcarbamate
Выход 66.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN(C(=O)OC(C)(C)C)c1ccc(OCCCN2C(=O)c3ccccc3C2=O)cc1
Reaction #65747
N-Boc-4-(3-phthalimidopropyloxy)phenylglycine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Cc2c(ncnc2Oc2ccc3[nH]ccc3c2)CN1C(=O)OC(C)(C)C
Reaction #73446
(±)-4-(1H-Indol-5-yloxy)-5,8-dihydro-6H-pyrido[3,4-d]pyrimidine-6,7-dicarboxylic acid 7-tert-butyl ester 6-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C1Cc2c(ncnc2Oc2ccc3c(ccn3C(=O)Nc3cc(C4CC4)on3)c2)CN1
Reaction #73447
(±)-4-[1-(5-Cyclopropyl-isoxazol-3-ylcarbamoyl)-1H-indol-5-yloxy]-5,6,7,8-tetrahydro-pyrido[3,4-d]pyrimidine-6-carboxylic acid methylamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](n2ccc(NC(=O)c3ccccc3)nc2=O)C[C@@H]1C(=O)OC(c1ccccc1)c1ccccc1
Reaction #79472
N-tert-butoxycarbonyl-cis-4-(N4-benzoylcytosin-1-yl)-D-proline diphenylmethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](Sc2ccc(Br)cc2Cl)CN1C(=O)OC(C)(C)C
Reaction #156713
(2S,4R)-4-(4-Bromo-2-chloro-phenylsulfanyl)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1C(=O)OCC(=O)C1=CC2SC(Br)=CC2S1
Reaction #159177
title compound
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)CO[C@@H]1[C@@H](Cc2ccccc2)COC[C@H](N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)C(=O)O[C@H]1C
Reaction #162919
tert-butyl N-[(3S,7S,8R,9S)-7-benzyl-9-methyl-8-(2-methylallyloxy)-2-oxo-1,5-dioxonan-3-yl]-N-tert-butoxycarbonylcarbamate
Выход 92.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CO[C@@H]1[C@@H](Cc2ccccc2)COC[C@H](N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)C(=O)O[C@H]1C
Reaction #162920
tert-butyl N-[(3S,7S,8R,9S)-7-benzyl-8-isobutoxy-9-methyl-2-oxo-1,5-dioxonan-3-yl]-N-tert-butoxycarbonylcarbamate
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1C(=O)OCC(=O)C1=CC2SC(Br)=CC2S1
Reaction #167120
title compound
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее