部分構造検索

OCc1ccccc1I

CC(C)(C=O)NC(=O)OC(C)(C)C
Reaction #6533
N-BOC-2-amino-2-methyl-1-propanal
収率 87.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(CCC=O)nc2ccccc21
Reaction #7191
title compound
収率 76.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCn2nc(-c3ccccn3)c(-c3ccnc4cc(Br)ccc34)c21
Reaction #8360
3-(7-Bromo-quinolin-4-yl)-2-pyridin-2-yl-5,6-dihydro-pyrrolo[1,2-b]pyrazol-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(CCO[Si](C)(C)C(C)(C)C)(C(=O)CC(=O)Cc2ccccc2)CC1
Reaction #8868
title product
収率 69.5%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1csc2c1CCCC2
Reaction #10320
4,5,6,7-tetrahydro-1-benzothiophene-3-carbaldehyde
収率 88.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCC(=O)c1ccncc1
Reaction #11584
titled compound
収率 87.8%DOI: 10.6084/m9.figshare.5104873.v1
O=CCCn1cc(C(F)(F)F)c(=O)[nH]c1=O
Reaction #40935
title compound
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CCCCn1cc(C(F)(F)F)c(=O)[nH]c1=O
Reaction #40937
title compound
収率 51.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1cn(CCC=O)c(=O)[nH]c1=O
Reaction #40942
title compound
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1cn(CCCC=O)c(=O)[nH]c1=O
Reaction #40944
title compound
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CC1(c2ccccc2)CCCC1
Reaction #41879
1-Phenyl-cyclopentanecarbaldehyde
収率 81.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C=O)NC(=O)OC(C)(C)C
Reaction #43536
desired product
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C=O)NC(=O)Cc1ccccc1
Reaction #43537
(S)-2-(benzylcarbonylamino)-propionaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](C=O)NC(=O)[C@@H](CC(=O)N1CCOCC1)c1ccc(F)cc1
Reaction #43564
2-(S)-(4-Fluoro-phenyl)-N-(1-(S)-formyl-2-methyl-propyl)-4-morpholin-4-yl-4-oxo-butyramide
収率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(c1ccc(C#N)cc1)n1cncc1C=O
Reaction #43696
methyl 3-[5-formyl-imidazol-1-yl]-3-(4-cyano-phenyl)-propionate
DOI: 10.6084/m9.figshare.5104873.v1
O=CC1c2c[nH]nc2CCN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44010
79
収率 81.9%DOI: 10.6084/m9.figshare.5104873.v1
O=CCc1cccc(N2CCOC2=O)c1
Reaction #44136
title compound
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CCCCCC2)CC1C=O
Reaction #44486
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc([N+](=O)[O-])cc(C(F)(F)F)c1
Reaction #45333
3-nitro-5-(trifluoromethyl)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(I)cc(C(F)(F)F)c1
Reaction #45336
3-iodo-5-(trifluoromethyl)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
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