Поиск подструктуры

12058

CCC(C)(CN=[N+]=[N-])NC(=O)OCc1ccccc1
Reaction #5652
1-Azido-2-(benyloxycarbonylamino)-2-methylbutane
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(OCc2cccc(F)c2)c(Br)c1
Reaction #6912
title compound
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(Cc2ccoc2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(Br)cc1F
Reaction #7428
compound ( 2 )
Выход 95.6%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2nn3c(c2-c2ccnc4cc(OCc5ccncc5)ccc24)CCC3)nc1
Reaction #8378
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@@H](Oc2cc(N)ccc2Cl)C1
Reaction #8727
title compound
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(/C=C\c2cc(OC)c(OC)c(OC)c2)cc1O
Reaction #8837
combretastatin A-4
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2c(C(=O)C(C)(C)C)oc3nc(-c4ccccc4Cl)c(-c4ccc(Cl)cc4)cc23)C(=O)C1=O
Reaction #8903
title compound
DOI: 10.6084/m9.figshare.5104873.v1
S=C1N(CCCc2ccncc2)CCN1CCc1ccccc1
Reaction #11565
titled compound
Выход 19.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40598
34
Выход 81.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1Cc2cc3c(cc2C[C@H]1C(=O)O)NC(=O)C(c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1)O3
Reaction #41848
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc2c(c1)NC(=O)[C@H](c1ccc(OCc3ccc(Cl)c(Cl)c3)cc1)O2)NC(=O)OC(C)(C)C
Reaction #41850
(S)-2-tert-Butoxycarbonylamino-3-{(S)-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl}-propionic acid methyl ester
Выход 56.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc2c(c1)N(C)C(=O)[C@H](c1ccc(OCc3ccc(Cl)c(Cl)c3)cc1)O2)NC(=O)OC(C)(C)C
Reaction #41851
(S)-2-tert-Butoxycarbonylamino-3-{(S)-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl}-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC2Cc3c(Cl)cc4c(c3O2)CCC4)cc1
Reaction #42227
(±)-(4-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methyl 4-methylbenzenesulfonate
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCC1Cc2cc(Cl)c3ccccc3c2O1
Reaction #42248
(±)-(5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methyl azide
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc2c(n[nH]1)OCCC2
Reaction #43424
product
Выход 79.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COc2cnc(COC(C)=O)cc2OCc2ccccc2)cc1
Reaction #43435
oil
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc2c(n[nH]1)OCC2
Reaction #43456
product
Выход 16.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Nc2ccc(Br)cc2F)c(-c2nnnn2CCC#N)cn(C)c1=O
Reaction #44201
desired product
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(Cl)cc1B(O)O)C(=O)O
Reaction #44376
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее