tributylphosphane

COC(=O)c1cc(N2CCOCC2)cc2c1nc(C)n2Cc1cccc(C(F)(F)F)c1C
Reaction #582
Ausbeute 0.0%750 AstraZeneca ELN dataset
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(Cc2ccoc2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7400
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc2c(Cl)cnnc2cc1OCc1ccncc1.Cl
Reaction #7572
4-chloro-6-methoxy-7-(4-pyridylmethoxy)cinnoline hydrochloride
Ausbeute 122.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(N2CCOCC2)c(F)c1
Reaction #8238
oil
Ausbeute 331.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #8240
solid
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(-n2ccnc2)c(F)c1
Reaction #8243
desired product
Ausbeute 158.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(-n2cnc(CO)c2)c(F)c1
Reaction #8245
desired product
Ausbeute 13.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc(-c2nn3c(c2-c2ccnc4ccccc24)OCC3)nc1
Reaction #8376
title compound
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)COc1ccc(OCCc2cccs2)cc1C
Reaction #9749
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)COc1ccc(SCc2coc(-c3ccc(C(F)(F)F)cc3)c2)cc1C
Reaction #9785
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)NCCCN(CCCc1ccccc1)S(=O)(=O)c1cccc2cnccc12
Reaction #10587
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)NCCCOc1cccc2c(Cl)nccc12
Reaction #10597
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(C(=O)O[C@H]2CC[C@@H](NC(=O)OC(C)(C)C)CC2)cc1
Reaction #10659
title compound
Ausbeute 96.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCC[PH+](CCCC)CCCC.c1ccc([B-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #42146
tri-n-butylphosphonium tetraphenylborate
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCSCCOc1cc(C)c(-c2cccc(COc3ccc4c(c3)OC[C@H]4CC(=O)OC)c2)c(C)c1
Reaction #43918
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)cc4COC(C)=O)c3)ccc21
Reaction #43930
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CSCCCOc1cc(C)c(Br)c(C)c1
Reaction #43938
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OC5CCS(=O)(=O)CC5)cc4C)c3)ccc21
Reaction #43943
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)c(C)c(OCCCS(C)(=O)=O)c(C)c4C)c3)ccc21
Reaction #43946
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)cc4C)c3)ccc21
Reaction #43948
title compound
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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