部分構造検索

COC(C)(C)C

CCN(CCCNC(=O)OC(C)(C)C)Cc1c2ccccc2cc2ccccc12
Reaction #41278
12b
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCCNCc1c2ccccc2cc2ccccc12
Reaction #41282
16
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)Nc1ccc(I)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #50916
405
収率 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)Nc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #50917
406
収率 75.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)Nc1ccc(-c2ccccc2SC)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #50919
409
収率 85.9%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(C2(OC)CC2)cc1
Reaction #52416
1-Ethynyl-4-(1-methoxycyclopropyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #70591
solid
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1csc(-c2cnc(-c3ccccc3)nc2)n1
Reaction #70592
title compound
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](C)N)C(=O)OCc2ccccc2)cc1
Reaction #87081
(S)-benzyl 2-((S)-2-aminopropanamido)-3-(4-methoxyphenyl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccn1)C(=O)OCc1ccccc1
Reaction #87188
(S)-benzyl 2-((tert-butoxycarbonyl)amino)-3-(pyridin-2-yl)propanoate
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](Cc1ccccn1)C(=O)OCc1ccccc1.O=C(O)C(F)(F)F
Reaction #87189
(S)-benzyl 2-amino-3-(pyridin-2-yl)propanoate TFA salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCCN(c2ccncc2NC(=O)c2csc(Br)n2)C1
Reaction #160786
(S)-tert-butyl 1-(3-(2-bromothiazole-4-carboxamido)pyridin-4-yl)piperidin-3-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc2c(c1)CCCN2)NC(=O)OC(C)(C)C
Reaction #161999
#214
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](Cc1ccc(-c2ccccn2)cc1)C(N)=O
Reaction #172089
(R)-tert-butyl 1-amino-1-oxo-3-(4-(pyridin-2-yl)phenyl)propan-2-ylcarbamate
収率 33.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cc(OCC(F)(F)F)c(C(F)(F)F)cc1NC(=O)CC(=O)c1cccc(-c2ccncc2)c1
Reaction #177526
DOI: 10.1039/C8SC04228D
CCOc1ccc2c(c1)N=C(c1cccc(-c3ccncc3)c1)CC(=O)N2
Reaction #177698
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C(Cc1ccccc1)n1cccc(N)c1=O
Reaction #178886
DOI: 10.1039/C8SC04228D
N#Cc1cc(C2=Nc3ccc(C#Cc4ccccc4)cc3NC(=O)C2)ccn1
Reaction #182738
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)CC(=O)c1cccc(-c2ccncc2)c1
Reaction #186739
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1cscc1NC(=O)c1ccc(CNCCCN2CCOCC2)cc1
Reaction #192780
DOI: 10.1039/C8SC04228D
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