子结构搜索

554606

CCOC(=O)C(Br)(Oc1cccc2[nH]ccc12)C(=O)OCC
Reaction #44843
7
收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1cccc2[nH]ccc12)C(=O)OCC
Reaction #44844
8
收率 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCNC(=O)OC(C)(C)C)OP(=O)(OC)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #58021
2-[(1-benzyloxycarbonylamino-2-methyl-propyl)-methoxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid methyl ester
收率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(NC(=O)OCc1ccccc1)P(=O)(O)OC(CCCNC(=O)OC(C)(C)C)C(=O)O
Reaction #58022
2-[(1-benzyloxycarbonylamino-2-methyl-propyl)-hydroxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid
收率 102.3%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(c2ccc(Cl)c(Cc3ccc(O)cc3)c2)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #87468
product
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(c2ccc(Cl)c(Cc3ccc(O)cc3)c2)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #87488
product
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1ccc2[nH]c(C)c(-c3ccc(OC)cc3)c2c1
Reaction #95111
2-[3-(4-Methoxy-phenyl)-2-methyl-1H-indole-5-yloxy]-2-methyl-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1ccc2[nH]c(C)c(-c3cccc(C)c3)c2c1
Reaction #95123
2-Methyl-2-[2-methyl-3-(3-methyl-phenyl)-1H-indole-5-yloxy]-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1ccc2[nH]c(C)c(-c3ccc(C)cc3)c2c1
Reaction #95125
2-Methyl-2-[2-methyl-3-(4-methyl-phenyl)-1H-indole-5-yloxy]-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1ccc2c(c1)c(CCc1ccccc1)c(C)n2C
Reaction #95127
2-Methyl-2-[1,2-dimethyl-3-(2-phenyl-ethyl)-1H-indole-5-yloxy]-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1ccc2[nH]c(C)c(-c3ccncc3)c2c1
Reaction #95132
2-Methyl-2-[2-methyl-3-(4-pyridyl)-1H-indole-5-yloxy]-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1ccc2[nH]c(C(C)C)c(-c3ccncc3)c2c1
Reaction #95133
2-[2-Isopropyl-3-(4-pyridyl)-1H-indole-5-yloxy]-2-methyl-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1ccc2[nH]c(Cc3ccccc3)c(-c3ccncc3)c2c1
Reaction #95134
2-[2-Benzyl-3-(4-pyridyl)-1H-indole-5-yloxy]-2-methyl-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1cccc2[nH]c(C)c(-c3ccccc3)c12
Reaction #95158
2-Methyl-2-[2-methyl-3-phenyl-1H-indole-4-yloxy]-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CCCn1c(C)c(-c2ccccc2)c2c(OC(C)(C)C(=O)OCC)cccc21
Reaction #95162
2-Methyl-2-[2-methyl-3-phenyl-1-propyl-1H-indole-4-yloxy]-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)[C@](C)(O)CN(Cc1ccc(-c2cc(Cl)ccc2F)cc1)NC(=O)c1cc(O)no1
Reaction #171388
title compound
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(OC(C)(C)C)c1c(C)nc2c(ccn2Cc2ccc(F)c(C)c2)c1-c1ccc(C)cc1
Reaction #183669
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(C)Oc1ccc2[nH]c(C(C)C)c(-c3ccncc3)c2c1
Reaction #184874
DOI: 10.1039/C8SC04228D
CCCCCC(C(C=CC(O)CCCCCCC(O[SiH](C)C)C(=O)OC(C)(C)C)C(C)(C)C)C(C)(C)C
Reaction #185230
DOI: 10.1039/C8SC04228D
CCOC(Cc1ccc(OCc2nc(C(C)(C)C)oc2C)cc1Cl)C(=O)O
Reaction #196739
DOI: 10.1039/C8SC04228D
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