Substructure Search

575739

COC(=O)CCNC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11725
title compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #11726
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ncc(Cl)cc1NC(=O)CCC(=O)O
Reaction #11771
title compound
Yield 31.2%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(/C=C/c2ccc(F)cc2)ccn1-c1ccc(OCCN2CCCC2)cc1
Reaction #43329
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(/C=C/c2ccn(-c3ccc(OCCN4CCCC4)cc3)c(=O)c2)cc1
Reaction #43333
title compound
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1C(=O)[C@H](N)CC1CCCCC1
Reaction #49774
H-DCha-Pro-OtBu
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C=O)cc(C(C)C)c1OCCN1CCOCC1
Reaction #52655
3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzaldehyde
Yield 14.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C=C2C(=O)Nc3ccc(Cl)cc32)cc(C(C)C)c1OCCN1CCOCC1
Reaction #52656
5-chloro-3-[3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzylidene]-1,3-dihydroindol-2-one
Yield 10.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C=C2C(=O)Nc3ccc(Br)cc32)cc(C(C)C)c1OCCN1CCOCC1
Reaction #52688
5-bromo-3-[3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzylidene]-1,3-dihydroindol-2-one
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CNCCN1CCc1ccc2c(c1)OCCO2
Reaction #67962
ethyl 1-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)piperazine-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(CCn2c(=O)cc(C)c3ccc(OC)cc32)CCN1CCc1ccc2c(c1)OCCO2
Reaction #68084
ethyl 1-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)-4-(2-(7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)ethyl)piperazine-2-carboxylate
Yield 64.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CC[C@H](NC(=O)OCc2ccccc2)[C@H](OC)C1)C(C)=O
Reaction #72092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)sc1C
Reaction #72093
title compound
Yield 7.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)CN1CCC[C@H]1C(=O)OC(C)(C)C
Reaction #82327
N-[[N-[N-(4-methylvaleryl)-L-asparaginyl]-L-phenylalanyl]methyl]-L-proline tert.butyl ester
Yield 27.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)CN1CCC[C@H]1C(=O)OC(C)(C)C
Reaction #82328
N-[[N-[N-(benzyloxycarbonyl)-L-alanyl]-L-phenylalanyl]methyl]-L-proline tert.butyl ester
Yield 36.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1
Reaction #82334
L-proline tert.butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1C[C@@H](O)[C@H](Cc1ccc(F)cc1)NC(=O)[C@H](CC(N)=O)NC(=O)OCc1ccccc1
Reaction #82347
N-[3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl]amino]-4-(4-fluorophenyl)-2(R)-hydroxybutyl]-L-proline tert.butyl ester
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C=CC(=O)N2CCCC[C@H]2C(=O)OCc2ccccc2)cc1
Reaction #82777
amide
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(=O)CCN1[C@@H](C)c1ccccc1
Reaction #89424
title compound
Yield 99.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@H]1CN2CCC1CC2)C(NCc1ccccc1)c1ccccc1
Reaction #164157
(R)-quinuclidin-3-yl 2-(benzylamino)-2-phenylacetate
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
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