部分構造検索

348627

CCOC(=O)C1CC(=O)C=CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44018
compound 103
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C(=CN(C)C)C(=O)C=CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44019
compound 104
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1c2cn[nH]c2C=CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44020
compound 105
収率 30.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(=O)CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44021
oil
収率 88.9%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1C[C@]1(N)C(=O)OCC.Cl
Reaction #46071
ethyl 1(R)-amino-2(S)-vinylcyclopropane carboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1C[C@]1(NC(=O)OC(C)(C)C)C(=O)O
Reaction #46084
title compound
収率 87.3%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1C[C@]1(N)C(=O)OC.Cl
Reaction #61359
compound 20b
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2ccc(Cl)cc2C2C=CCC12
Reaction #75641
Compound 3
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(=C/CC[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@H](C)C(=O)OC)NC(=O)OC(C)(C)C
Reaction #80535
desired product 47c
収率 70.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=C1C[C@H](C(=O)OC(C)(C)C)[C@@H](C(=O)OCc2ccccc2)N(C(=O)OCc2ccccc2)C1
Reaction #89705
1,2-dibenzyl 3-tert-butyl(2S,3S)-5-(2-methoxy-2-oxoethylidene)piperidine-1,2,3-tricarboxylate
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CN[C@H](C(=O)O)[C@@H](C(=O)OC(C)(C)C)C1
Reaction #89706
(2S,3S)-3-(tert-butoxycarbonyl)-5-(2-methoxy-2-oxoethyl)piperidine-2-carboxylic acid
収率 88.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1CC1(NC(=O)C1CC2CC1C(=O)O2)C(=O)OCC
Reaction #180836
DOI: 10.1039/C8SC04228D
C=CCCCCCN(NC(=O)OC(C)(C)C)C(=O)N1CC(Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)CC1C(=O)NC1(C(=O)OCC)CC1C=C
Reaction #182583
DOI: 10.1039/C8SC04228D
COc1ccc2c(OC3CC4C(=O)NC5(C(=O)O)CC5C=CCCCCN(C)C(=O)C4C3)cc(-c3csc(C4CCCCC4)n3)nc2c1C
Reaction #185264
DOI: 10.1039/C8SC04228D
C=CC1CC1(NC(=O)C1CC(Oc2nc(-c3ccccc3)nc3cc(OC)ccc23)CC1C(=O)O)C(=O)OCC
Reaction #192517
DOI: 10.1039/C8SC04228D
C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(OC(=O)N2Cc3cccc(F)c3C2)CC1C(=O)NC1(C(=O)OCC)CC1C=C
Reaction #192767
DOI: 10.1039/C8SC04228D
COc1ccc2c(OC3CC4C(=O)NC5(C(=O)O)CC5C=CCCCCN(C)C(=O)C4C3)cc(-c3cccc(C(C)C)n3)nc2c1C
Reaction #197843
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)N2CC=CCC(NC(=O)NCc3ccccc3)C2C(=O)OC(C)(C)C)cc1
Reaction #208556
DOI: 10.1039/C8SC04228D
C=CC1CC1(NC(=O)C1CC(Oc2nc(-c3ccc(OC)cc3)nc3c(C)c(OC)ccc23)CC1C(=O)O)C(=O)OCC
Reaction #209674
DOI: 10.1039/C8SC04228D
C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(OC(=O)N2Cc3cccc(F)c3C2)CC1C(=O)NC1(C(=O)OCC)CC1C=C
Reaction #211552
DOI: 10.1039/C8SC04228D
1 ページ次のページ