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1328994

O=C(CCCCl)NCCc1cccc2ccc(S(=O)CC3CC3)cc12
Reaction #256350
DOI: 10.1039/C8SC04228D
COc1ccc2cccc(CCNC(=O)CCCCl)c2c1
Reaction #284480
DOI: 10.1039/C8SC04228D
N#Cc1ccc(C[C@@H](C#N)NC(=O)[C@H](CC(Cl)Cl)N[C@@H](c2ccc(Br)cc2)C(F)(F)F)c(F)c1
Reaction #327036
(2S)-2-{[(1S)-1-(4-bromophenyl)-2,2,2-trifluoroethyl]amino}-4,4-dichloro-N-[(1S)-1-cyano-2-(4-cyano-2-fluorophenyl)ethyl]butanamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)C1(CC(=O)O)CCCC1
Reaction #420482
(S)-2-(1-(3-(biphenyl-4-yl)-1-(dimethylamino)-1-oxopropan-2-ylcarbamoyl)cyclopentyl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)C1(CC(=O)O)CCCC1
Reaction #420483
(S)-2-(1-(3-(biphenyl-4-yl)-1-(methylamino)-1-oxopropan-2-ylcarbamoyl)cyclopentyl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nnnc1[C@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)C1(CC(=O)O)CCCC1
Reaction #420484
(S)-2-(1-(2-(biphenyl-4-yl)-1-(1-methyl-1H-tetrazol-5-yl)ethylcarbamoyl)cyclopentyl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cl)CC1(C(=O)N[C@@H](Cc2ccc(-c3ccccc3)cc2)C(=O)N(C)C)CCCC1
Reaction #420529
(S)—N-(3-(biphenyl-4-yl)-1-(dimethylamino)-1-oxopropan-2-yl)-1-(2-chloroallyl)cyclopentanecarboxamide
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cl)CC1(C(=O)N[C@@H](Cc2ccc(-c3ccccc3)cc2)C(=O)NC)CCCC1
Reaction #420532
(S)—N-(3-(biphenyl-4-yl)-1-(methylamino)-1-oxopropan-2-yl)-1-(2-chloroallyl)cyclopentanecarboxamide
Ausbeute 49.7%DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cl)CC1(C(=O)N[C@@H](Cc2ccc(-c3ccccc3)cc2)C(=O)N(C)Cc2ccco2)CCCC1
Reaction #420535
(S)—N-(3-(biphenyl-4-yl)-1-((furan-2-ylmethyl)(methyl)amino)-1-oxopropan-2-yl)-1-(2-chloroallyl)cyclopentanecarboxamide
Ausbeute 71.2%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)CCN1CCCC21
Reaction #457153
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(C(=O)Nc2ccc(C[C@H](NC(=O)C3(C)CC3(Cl)Cl)C(=O)O)cc2)c(C)c1
Reaction #480622
N-[(2,2-dichloro-1-methylcyclopropyl)carbonyl]-4-[[(2,4,6-trimethylphenyl)carbonyl]amino]-L-phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(=O)N[C@@H](Cc2ccc(NC(=O)N3CCC(C#N)(c4ccccc4)CC3)cc2)C(=O)O)CC1(Cl)Cl
Reaction #480624
4-[[(4-cyano-4-phenyl-1-piperidinyl)carbonyl]amino]-N-[(2,2-dichloro-1-methylcyclopropyl)carbonyl]-L-phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCl)NC1CCc2cc3c(cc2C1)OCC3
Reaction #563950
7-(4-Chlorobutyramido)-2,3,5,6,7,8-hexahydronaphtho[2,3-b]furan
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cccc(CCNC(=O)CCCCl)c2c1
Reaction #570578
N-[2-(7-Methoxynaphth-1-Yl)Ethyl]-4-Chlorobutyramide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cccc(CCN3CCCC3=O)c2c1
Reaction #570579
N-[2-(7-Methoxynaphth-1-Yl)Ethyl]Pyrrolidin-2-One
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCl)NCCc1ccccc1
Reaction #608923
HJC-1-48
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1CCc1ccccc1
Reaction #608924
1-Phenethyl-pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)CCN1CCCC21
Reaction #670453
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(=O)NC(Cc2ccc(NC(=O)N3CCC(C#N)(c4ccccc4)CC3)cc2)C(=O)O)CC1(Cl)Cl
Reaction #752001
DOI: 10.1039/C8SC04228D
C[C@@H]1CC(=O)N[C@H]1Cc1ccccc1
Reaction #936241
title material
Ausbeute 32.1%DOI: 10.6084/m9.figshare.5104873.v1
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