子结构搜索

CCOC(=O)NCCCl

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Reaction #40684
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1cc(F)cc(F)c1)C(=O)Cl
Reaction #51499
t-butyl-(1S)-2-chloro-1-[3,5-difluorobenzyl]-2-oxoethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2Cl)nc1Cl
Reaction #72118
title compound
收率 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](Cl)C2)nc1C
Reaction #72119
title compound
收率 40.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(c2ccncc2)(c2ccc(Cl)cc2)CC1
Reaction #73840
title compound
收率 0.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](CCC(=O)OCc1ccccc1)COc1cc(C#N)ccc1I
Reaction #78201
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)NCCOc1ccc2c(c1)C(C)(C)c1[nH]c3cc(C#N)ccc3c1C2=O
Reaction #89988
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCOc1ccc(-c2cccc3cnc(NC4CCC(O)CC4)nc23)cc1)C(=O)OC(C)(C)C
Reaction #182223
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCC(Cl)c1cccs1
Reaction #187083
DOI: 10.1039/C8SC04228D
CCOC(=O)N(CCc1cccs1)CC(=O)Cl
Reaction #189014
DOI: 10.1039/C8SC04228D
CCOC(=O)NCCOc1ccc([N+](=O)[O-])cc1
Reaction #190041
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(COc1cccc(C#N)c1)Cc1ccc(I)cc1
Reaction #194099
DOI: 10.1039/C8SC04228D
O=C(OCCN1CCOC1=O)c1ccccc1Nc1ccnc2c(C(F)(F)F)cccc12
Reaction #200010
DOI: 10.1039/C8SC04228D
O=C1CC2CCN(C(=O)OCc3ccccc3)C2C1
Reaction #202687
DOI: 10.1039/C8SC04228D
CCCCCCCCN1CCN(CCO)C1=O
Reaction #202787
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(C#N)(c2cccnc2)CC1
Reaction #204896
DOI: 10.1039/C8SC04228D
C=CCOC(=O)NCC(=O)Cl
Reaction #205359
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(C#N)(c2ccc(Cl)c(F)c2)CC1
Reaction #211663
DOI: 10.1039/C8SC04228D
CCOC(=O)NCC(Cl)(Cl)Cl.N[C@@H]1C=CC[C@H]1O
Reaction #214971
trans-3-amino-4-hydroxy-cyclopentene N-trichloroethyl urethane
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCCN1CCn1ccnc1[N+](=O)[O-]
Reaction #221248
DOI: 10.1039/C8SC04228D
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