部分構造検索

18332

CCOC(=O)C=Cc1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12015
desired compound
収率 91.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1ccc(C=O)cn1
Reaction #71634
title compound
収率 93.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC[C@H](NC(=O)OC(C)(C)C)C(=O)OC
Reaction #86651
(S)-3-Allyloxy-2-tert-butoxycarbonylamino-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(c2ccccc2)CCCCC1=O
Reaction #158426
2-allyl-2-phenylcyclohexanone
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1COCCC1=O
Reaction #160815
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1nc(C#N)cc2ncn(Cc3ccc(C(F)(F)F)cc3)c12)C1CCC1
Reaction #168265
(R)-4-((1-cyclobutylethyl)amino)-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217190
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217191
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217192
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217193
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217194
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217195
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217196
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217197
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217198
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217199
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217200
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217201
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217202
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)cc2)cc1
Reaction #217203
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