子结构搜索

440409

COC(=O)C1c2ccccc2CN1C(=O)OC(C)(C)C
Reaction #52158
N-BOC-1,3-dihydro-2H-isoindol-1-carboxylic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)c2ccccc2CN1C(=O)OC(C)(C)C
Reaction #52159
N-BOC-1-methyl-1,3-dihydro-2H-isoindol-1-carboxylic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)c1ccc(C(NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #61088
tert-butoxycarbonylamino-[4-(diethoxy-phosphoryl)-phenyl]-acetic acid benzyl ester
收率 93.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #61096
solid
收率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #61099
solid
收率 14.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1csc(NC(=O)[C@@H](NC(=O)[C@H](NC(=O)OC(C)(C)C)c2ccc3c(c2)OCCO3)[C@@H](C)c2ccccc2)n1
Reaction #61107
2-{(2S,3S)-2-[(R)-2-tert-butoxycarbonylamino-2-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-acetylamino]-3-phenyl-butyrylamino}-thiazole-4-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](NC(=O)OC(C)(C)C)C(=O)O)cc1C
Reaction #61111
(R)-tert-butoxycarbonylamino-(4-methoxy-3-methyl-phenyl)-acetic acid
收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1csc(NC(=O)[C@@H](NC(=O)C(NC(=O)OC(C)(C)C)c2ccc(SC)cc2)[C@@H](C)c2ccccc2)n1
Reaction #61112
2-{(2S,3S)-2-[2-tert-butoxycarbonylamino-2-(4-methylsulfanyl-phenyl)-acetylamino]-3-phenyl-butyrylamino}-thiazole-4-carboxylic acid methyl ester
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #72928
solid
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@](C)(C(=O)N1CCOCC1)c1ccccc1
Reaction #72929
N-(tert-butoxycarbonyl)-(1S)-1-methyl-2-morpholin-4-yl-2-oxo-1-phenylethylamine
收率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NC(C(=O)O[C@H]1CN2CCC1CC2)c1ccccc1
Reaction #164158
(R)-quinuclidin-3-yl 2-amino-2-phenylacetate di-hydrochloride
收率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1nc(-c2ccc(-c3ccc(C(=O)CNC(=O)C4c5ccccc5CN4C(=O)OC(C)(C)C)cc3)cc2)c[nH]1)C(C)C
Reaction #167087
crude material
收率 111.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(NC(=O)OC(C)(C)C)(c1cccc(Br)c1)C(F)(F)F
Reaction #168731
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(CO)(c1cccc(Br)c1)C(F)(F)F
Reaction #168732
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1cc(C(=O)c2cncc(NC(=O)C(NC(=O)OC(C)(C)C)c3ccc(Cl)cc3)c2)c2cncnc21
Reaction #169506
title compound
收率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OCCOc1ccc(C(NC(=O)OC(C)(C)C)C(=O)O)cc1
Reaction #174494
DOI: 10.1039/C8SC04228D
COC(=O)C1CSC2CC(NC(=O)OC(C)(C)C)(c3ccccc3)C(=O)N21
Reaction #180097
DOI: 10.1039/C8SC04228D
CCOP(=O)(OCC)c1ccc(C(NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #180105
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(C(=O)OCC(=O)c1ccccc1)c1ccc(O)cc1
Reaction #196457
DOI: 10.1039/C8SC04228D
COC(=O)C(NC(=O)OC(C)(C)C)c1ccc(-c2c(OC)cccc2OC)cc1
Reaction #206152
DOI: 10.1039/C8SC04228D
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