部分構造検索

3699

CCOC(=O)C(CC)N=Cc1ccccc1
Reaction #945
desired product
収率 88.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CCC(c2ccc(Cl)cc2)=N1
Reaction #44622
title compound
収率 91.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CCC(c2cc(F)c(F)c(F)c2)=N1
Reaction #44659
titled compound
収率 80.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CC[C@@H](c2cc(F)c(F)c(F)c2)N1
Reaction #44660
titled compound
収率 95.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC1(F)CCCC1)N=C(c1ccccc1)c1ccccc1
Reaction #47455
2-(benzhydrylidene-amino)-3-(1-fluoro-cyclopentyl)-propionic acid ethyl ester
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(N)CC1(F)CCCC1
Reaction #47456
2-amino-3-(1-fluoro-cyclopentyl)-propionic acid ethyl ester
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](CC(C)CC)N=C(c1ccccc1)c1ccccc1
Reaction #47683
(S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(c2ccc(OC)c(C)c2C)N1
Reaction #176912
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCC(c2cc(F)c(F)c(F)c2)=N1
Reaction #184147
DOI: 10.1039/C8SC04228D
CCOC(=O)CC1(C(=O)OCC)N=C(c2ccccc2OC)N(C)O1
Reaction #195257
DOI: 10.1039/C8SC04228D
CCOC(=O)C(N)CC=C1CCOCC1
Reaction #196261
DOI: 10.1039/C8SC04228D
CCOC(=O)C(N)Cc1cccc(OC)n1
Reaction #201017
DOI: 10.1039/C8SC04228D
CCOC(=O)C(N)Cc1nc(-c2ccccc2)ccc1NC(=O)OC(C)(C)C
Reaction #213528
DOI: 10.1039/C8SC04228D
CCOC(=O)C(N)Cc1ccc(OCCc2nc(-c3ccccc3)oc2C)c2ccccc12
Reaction #225266
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Cc1ccc(-c2ccno2)cc1)N=C(c1ccccc1)c1ccccc1
Reaction #225707
DOI: 10.1039/C8SC04228D
CCOC(=O)C(N)Cc1ccc(-c2ccno2)cc1
Reaction #243441
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(N)CC2CCC(C1)O2
Reaction #255555
DOI: 10.1039/C8SC04228D
CCOC(=O)C(N)CC1(F)CCCC1
Reaction #259492
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCC#N)(N=Cc1ccccc1)C(F)F
Reaction #266407
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C(CC1CCCCCCC1)N=C(c1ccccc1)c1ccccc1
Reaction #272054
DOI: 10.1039/C8SC04228D
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