331 件の反応に参加

11878

N#CC1(c2ccc(Cl)cc2)CCOCC1
Reaction #7910
4-(4-chlorophenyl)tetrahydropyran-4-carbonitrile
収率 95.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#CC1(C#N)CCOCC1
Reaction #40784
solid
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)C1(C#N)CCOCC1
Reaction #44853
title compound
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1OCCOCCBr
Reaction #48961
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1N=C(N[C@H]2C[C@@H]3CC[C@H]2C3)SC12CCOCC2
Reaction #74400
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N#CC1(c2ccc(Cl)cc2)CCOCC1
Reaction #75554
4-(4-chlorophenyl)tetrahydropyran-4-carbonitrile
収率 95.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)C1(C(=O)OCC)CCOCC1
Reaction #77318
title compound
収率 61.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1(C)OB(c2cccc(N3CCOCC3)c2)OC1(C)C
Reaction #85807
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc2c(c1)C1(CCOCC1)C(=O)CC2
Reaction #90094
title compound
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
c1ccc(CN2CCC(N3CCOCC3)CC2)cc1
Reaction #178673
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C2(C#N)CCOCC2)c1
Reaction #179452
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(CCOCCBr)c1c(Cl)cccc1I
Reaction #185871
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC1(c2ccc(Cl)c(Cl)c2)CCOCC1
Reaction #192432
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)COc1ccc2ccc(OCCOCCBr)c(C(C)=O)c2c1
Reaction #203646
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C1(c2ccccc2OCCOCCBr)Sc2ccccc2N(C)C1=O
Reaction #207081
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC1(C#N)CCOCC1
Reaction #247799
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#CC1(c2ccc(OCCCN3CCCC3)cc2)CCOCC1
Reaction #248526
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1OCCOCCBr
Reaction #250203
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2c(Nc3ccc(Cl)cc3F)ncnc2cc1OCCOCCBr
Reaction #262165
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1N=C(NC2CC3CCC2C3)SC12CCOCC2
Reaction #264421
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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