子结构搜索

10372

CC(C)(O)Cn1ccc(NC(=O)C(CC2CCOCC2)NC(=O)OC(C)(C)C)n1
Reaction #47251
[1-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-ylcarbamoyl]-2-(tetrahydro-pyran-4-yl)-ethyl]-carbamic acid t-butyl ester
收率 93.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)Cn1ccc(NC(=O)C(CC2CCOCC2)NC(=O)OC(C)(C)C)n1
Reaction #47692
[1-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-ylcarbamoyl]-2-(tetrahydro-pyran-4-yl)-ethyl]-carbamic acid t-butyl ester
收率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)OC(C)(C)C)C(=O)Nc1ccn(CC(C)(C)O)n1
Reaction #47696
{(S)-1-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-ylcarbamoyl]-3-methyl-butyl}-carbamic acid t-butyl ester
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](N)C(=O)O.COc1ccc2c3c1O[C@H]1C(=O)CC[C@H]4[C@@H](C2)N(C)CC[C@]314
Reaction #60611
solid
收率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)OC(C)(C)C
Reaction #60616
Boc-Leu-Glu-OtBu
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)OC(C)(C)C)C(=O)Oc1cc(Cl)c(Cl)cc1Cl
Reaction #81363
N-(1,1-dimethylethoxycarbonyl)leucine 2,4,5-trichlorophenyl ester
收率 100.6%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@H](CC1CCCCC1)NC(=O)OC(C)(C)C
Reaction #87110
(S)-tert-Butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate
收率 105.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1(CO)CN(CC23CC4CC(CC(C4)C2)C3)C(=O)N1
Reaction #162349
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(C(=O)OCC(=O)c2ccc3c(c2)COc2cc4c(cc2-3)CCCC4=O)N(C(=O)OC(C)(C)C)C1
Reaction #182710
DOI: 10.1039/C8SC04228D
CCOC(=O)CSCC1C(C(=O)OCC)C1C(NC(=O)OC(C)(C)C)C(=O)OCC
Reaction #196865
DOI: 10.1039/C8SC04228D
CC1CC(C(=O)OC2CCc3cc4c(cc3C2=O)OCc2cc(Cl)ccc2-4)N(C(=O)OC(C)(C)C)C1
Reaction #199320
DOI: 10.1039/C8SC04228D
COC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)NC(=O)OC(C)(C)C
Reaction #217167
product
收率 96.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(F)[C@@H]2C[C@@H](NCc3ccc(Cl)c(Cl)c3)[C@@](NC(=O)OC(C)(C)C)(C(=O)OCC)[C@@H]21
Reaction #217691
(1R,2R,3R,5R,6R)-2-t-butoxycarbonylamino-3-(3,4-dichlorobenzylamino)-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester
收率 39.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)[C@H]2[C@@H](C[C@H]1NCc1ccc(Cl)c(Cl)c1)[C@]2(F)C(=O)OCC
Reaction #217692
(1R,2R,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzylamino)-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester
收率 92.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(NC(=O)OC(C)(C)C)C1C(CNC(=O)c2cccc(Cl)c2)C1C(=O)OCC
Reaction #232101
DOI: 10.1039/C8SC04228D
CC(C)C(COCc1ccccc1)CC(CO)NC(=O)OC(C)(C)C
Reaction #235583
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1(C(=O)OCc2ccccc2F)CC(O)C2C(C(=O)OCc3ccccc3F)C21
Reaction #248247
DOI: 10.1039/C8SC04228D
CCOC(=O)C(NC(=O)OC(C)(C)C)C1C(CN=[N+]=[N-])C1C(=O)OCC
Reaction #249524
DOI: 10.1039/C8SC04228D
COC(=O)C(CC1CCC(=O)CC1)NC(=O)OC(C)(C)C
Reaction #254694
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(c2ccc(-c3nc4ccc(C5(c6ccccc6)CC5)nc4s3)c(F)c2)CC1C(=O)O
Reaction #270323
DOI: 10.1039/C8SC04228D
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