9-borabicyclo[3.3.1]nonane

CCOC(CCCc1cc(C(=O)NC2CC2)ccc1F)OCC
Reaction #6968
N-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamide
收率 93.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(C4CC4)nc3N21
Reaction #12014
desired product
收率 35.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(Cl)cc2c1CCC2
Reaction #42221
6-chloro-4-methoxyindane
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN1CCOc2c(I)cc(C(=O)OC)cc21
Reaction #42465
title compound
收率 91.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN1CCOc2ccc(C(=O)OC)cc21
Reaction #42496
title compound
收率 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(COc2cc(CCc3ccc(F)cc3)ccn2)cc1
Reaction #43334
title compound
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])c1ccc(-c2nn(CCCO)cc2-c2ccnc3c2ccn3S(=O)(=O)c2ccccc2)cc1
Reaction #57214
title compound
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCCC[C@@H](CC[C@@H]1[C@@H](Cc2cccc(OCc3ccccc3)c2)[C@@H](CO)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #67888
titled compound
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCCC(NS(=O)C(C)(C)C)C1(c2ccc(F)cc2)CCC2(CC1)OCCO2
Reaction #73478
title compound ( 107 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
OCCc1ccc2c(c1)CCCO2
Reaction #76472
6-(2-hydroxyethyl)chroman
收率 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(NCCCc1ccc(Br)cc1)OCc1ccccc1
Reaction #76650
N-[3-(4-bromophenyl)propyl](phenylmethoxy)carboxamide
收率 54.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(NCCCc1ccc(CCNC(=O)OCc2ccccc2)cc1)OCc1ccccc1
Reaction #76651
(phenylmethoxy)-N-[3-(4-{2-[(phenylmethoxy)carbonylamino]ethyl}phenyl)propyl]carboxamide
收率 35.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C1Nc2cc(CC3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCC[C@@H]12
Reaction #156900
(S)-3-((1-(4-chlorophenyl)piperidin-4-yl)methyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N1CCN(C(=O)OCc2ccccc2)C(CCc2cccnc2)C1
Reaction #157314
desired product
收率 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccccc1CCCNC(=O)OC(C)(C)C
Reaction #163945
methyl 2-(3-(tert-butoxycarbonylamino)propyl)benzoate
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc([N+](=O)[O-])ccc1-n1cccc(CCO)c1=O
Reaction #172383
3-(2-Hydroxyethyl)-1-(2-methyl-4-nitrophenyl)pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc([N+](=O)[O-])ccc1-n1cccc(CCO)c1=O
Reaction #172389
3-(2-Hydroxyethyl)-1-(2-methoxy-4-nitrophenyl)pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCc1cc([N+](=O)[O-])ccc1-n1cccc(CCO)c1=O
Reaction #172396
3-(2-Hydroxyethyl)-1-[2-(methoxymethyl)-4-nitrophenyl]pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc([N+](=O)[O-])ccc1-n1cccc(CCCO)c1=O
Reaction #172400
3-(3-Hydroxypropyl)-1-(2-methyl-4-nitrophenyl)pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc([N+](=O)[O-])cc(C)c1-n1cccc(CCO)c1=O
Reaction #172407
1-(2,6-Dimethyl-4-nitrophenyl)-3-(2-hydroxyethyl)pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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