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1223672

C[C@@H](C(=O)N1CCC[C@H](NC(=O)OCc2ccccc2)C1)N1CC[C@H](NS(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7385
title compound
収率 42.5%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(=O)NC1CCCN(C(=O)[C@H](C)N2CC[C@H](NS(=O)(=O)c3ccc4cc(Cl)ccc4c3)C2=O)C1
Reaction #7399
title compound
収率 115.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCC[C@H](NC(=O)OCc2ccccc2)C1)N1CC[C@H](NS(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7414
title compound
収率 42.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCC[C@H](N)C1)N1CC[C@H](NS(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7415
title compound
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(CCN2CCOCC2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O.O=CO
Reaction #7420
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(CCN2CCOCC2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O.O=CO
Reaction #61717
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1CN(CC(=O)Nc2c(Cl)cccc2Cl)CCN1
Reaction #63612
3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-1-piperazineacetamide
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CCCBr)COC1CCCCO1
Reaction #79372
expected product
収率 108.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)CN2CCOCC2)C(=O)N[C@@H](CC2=CCCC2)C(=O)[C@@]2(C)CO2)cc1
Reaction #87084
(S)-N-((S)-3-(cyclopent-1-en-1-yl)-1-((R)-2-methyloxiran-2-yl)-1-oxopropan-2-yl)-3-(4-methoxyphenyl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanamide
収率 43.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@H](C)NC(=O)CN2CCOCC2)C(=O)N[C@@H](CC2CCCC2)C(=O)[C@@]2(C)CO2)cc1
Reaction #87086
(2S,3R)-N-((S)-3-cyclopentyl-1-((R)-2-methyloxiran-2-yl)-1-oxopropan-2-yl)-3-hydroxy-3-(4-methoxyphenyl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanamide
収率 61.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)CN1CCOCC1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](Cc1ccccc1)C(=O)[C@@]1(C)CO1
Reaction #87187
(S)-3-cyclopropyl-N-((S)-1-((R)-2-methyloxiran-2-yl)-1-oxo-3-phenylpropan-2-yl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanamide
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #93647
B7
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N[C@@H](C)C(=O)N[C@H](C(=O)N1CCC[C@H]1C(=O)Nc1cc2c(Nc3ccc(F)c(Cl)c3F)ncnc2cc1OC)C(C)(C)C.Cl
Reaction #162890
title compound
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CC2N(C(=O)C(NC(=O)c3ccc(C(F)(F)F)nc3)CN2S(=O)(=O)c2ccc(Cl)cc2Cl)C(Cc2ccc(Cl)cc2)C1=O
Reaction #179255
DOI: 10.1039/C8SC04228D
COC1OCCC1NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)c1ccc2c(c1)Nc1ccccc1S2
Reaction #179822
DOI: 10.1039/C8SC04228D
CC=Cc1cc(C(OCc2ccccc2)(C(F)(F)F)C(F)(F)F)ccc1N1CCN(C(=O)CN2C(=O)NC(C)(c3cnc4c(c3)OCCO4)C2=O)CC1
Reaction #182450
DOI: 10.1039/C8SC04228D
CC(C)N(CCNS(C)(=O)=O)C(=O)C(C)N1CCC(NS(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #186407
DOI: 10.1039/C8SC04228D
CNC(=O)C(Cc1ccc2ccccc2c1)N1CCN(C(=O)C(Cc2ccc(F)cc2)NC(=O)C2CCCN2C(=O)OC(C)(C)C)C(COC)C1
Reaction #202338
DOI: 10.1039/C8SC04228D
Cc1cc(N2CCN(C3CNC(C(=O)N4CCSC4)C3)CC2)n(-c2ccccc2)n1
Reaction #203990
DOI: 10.1039/C8SC04228D
COc1ccc(Cl)cc1S(=O)(=O)N1CC(NC(=O)C2CC2)C(=O)N2C(Cc3ccc(Cl)cc3)C(=O)N(C(C)C)CC21
Reaction #213801
DOI: 10.1039/C8SC04228D
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