بحث البنية الفرعية

BrCc1ccccc1

N=C(NC(=O)OCc1ccccc1)c1ccc(CN)cc1
Reaction #953
4-aminomethyl-1-(N-benzyloxycarbonylamidino)benzene
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(-c2ccc(Cn3cccc3)cc2)cc2onc(-c3ccccc3)c2c1=O
Reaction #8409
desired compound
المردود 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](c1ccccc1)N1Cc2cc3c(cc2C[C@H]1C(=O)O[C@@H]1C[C@H](C)CC[C@H]1C(C)C)N(C)C(=O)[C@H](c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1)O3
Reaction #41891
(3S,7S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-1-methyl-2-oxo-6-((S)-1-phenyl-propyl)-2,3,5,6,7,8-hexahydro-1H-4-oxa-1,6-diaza-anthracene-7-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](c1ccccc1)N1Cc2cc3c(cc2C[C@H]1C(=O)O[C@@H]1C[C@H](C)CC[C@H]1C(C)C)N(C)C(=O)[C@H](c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1)O3
Reaction #41896
(3S,7S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-1-methyl-2-oxo-6-((S)-1-phenyl-propyl)-2,3,5,6,7,8-hexahydro-1H-4-oxa-1,6-diaza-anthracene-7-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](c1ccccc1)N1Cc2cc3c(cc2C[C@H]1C(=O)O[C@@H]1C[C@H](C)CC[C@H]1C(C)C)N(C)C(=O)[C@H](c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1)O3
Reaction #41901
(3S,7S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-1-methyl-2-oxo-6-((S)-1-phenyl-propyl)-2,3,5,6,7,8-hexahydro-1H-4-oxa-1,6-diaza-anthracene-7-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CO)cc1
Reaction #44329
4-cyanobenzyl alcohol
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(F)(F)F)cc1CNCc1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #45310
[2-amino-5-(trifluoromethyl)benzyl][3,5-bis(trifluoromethyl)benzyl]amine
المردود 24.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45329
EtOAc hexanes
المردود 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1Br
Reaction #47824
titled compound
المردود 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OC
Reaction #47825
titled compound
المردود 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OCC
Reaction #47826
titled compound
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC1C(C(=O)OCC)=C(c2ccccc2)c2ccc(OC)cc21
Reaction #47841
titled compound
المردود 75.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1N1CCOCC1
Reaction #47842
titled compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1NCc1ccccc1
Reaction #47843
titled compound
المردود 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1NC1CCCCC1
Reaction #47844
titled compound
المردود 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)c1ccc(CBr)cc1
Reaction #52068
2-(4-bromomethyl-phenyl)-2-methyl-propionic acid ethyl ester
المردود 97.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)c1ccc(CN(Cc2cccc(OCC(=O)OC(C)(C)C)c2)S(=O)(=O)c2cccnc2)cc1
Reaction #52071
2-(4-{[(3-tert-butoxycarbonylmethoxy-benzyl)-(pyridine-3-sulfonyl)-amino]-methyl}-phenyl)-2-methyl-propionic acid ethyl ester
المردود 48.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2CBr)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52926
N-(2,6-dichlorobenzoyl)-4-[2-(bromomethyl)phenyl]-L-phenylalanine methyl ester
المردود 70.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(C)CCCc2ccccc2)c1
Reaction #54363
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(C(CC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #64493
desired material
المردود 50.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي