phosphane

CCCCCCCCOP(Cl)Cl
Reaction #53631
Octylphosphorodichloridite
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(Nc1ccc(CCBr)cc1)C(F)(F)C(F)(F)C(F)(F)F
Reaction #63303
2,2,3,3,4,4,4-heptafluoro-N-[4-(2-bromoethyl)phenyl]butanamide
Rendimiento 54.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCC[P+](CCCC)(CCCC)C(C)C(=O)O.[Cl-]
Reaction #94546
Tri-n-butyl(1-carboxyethyl)phosphonium Chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CCCC[P+](CCCC)(CCCC)CC(=O)O.[Cl-]
Reaction #94547
Tri-n-butyl(carboxymethyl)phosphonium Chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
—
Reaction #160400
solid
Rendimiento 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1(C)CCC(=O)CC(C)(C)P1c1ccccc1-c1ccccc1
Reaction #166163
title compound
Rendimiento 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)c1cc(C(C)C)c(-c2ccccc2P2C(C)(C)CCC(=O)CC2(C)C)c(C(C)C)c1
Reaction #166165
title compound
Rendimiento 63.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(NS(C)(=O)=O)cc1
Reaction #166170
N-p-tolylmethanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(NC(=O)Nc2ccccc2)cc1
Reaction #166171
1-Phenyl-3-p-tolylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc([N+](=O)[O-])cc1
Reaction #166172
4-Nitrobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(N2CCOCC2)cc1
Reaction #166175
4-Tolylmorpholine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N(CC(=O)O)C1CCOCC1
Reaction #167560
2-(tert-butoxycarbonyl(tetrahydro-2H-pyran-4-yl)amino)acetic acid
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(OS(=O)(=O)C2CC2)cc1
Reaction #181906
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(CCBr)cc1)C(F)(F)C(F)(F)C(F)(F)F
Reaction #221244
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(O)c1ccccc1
Reaction #228078
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1cn(-c2ccc(N3CC(Cn4nnc(C)n4)OC3=O)cc2F)nn1
Reaction #237904
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CP(C)C1CCCCC1
Reaction #250269
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=P(c1ccccc1)(c1ccccc1)c1ccc2ccccc2c1-c1c(O)ccc2ccccc12
Reaction #252394
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#CCCSC1c2ccccc2COc2ccc(OCc3ccc4ccc(Cl)cc4n3)cc21
Reaction #261545
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)c1cc(-c2ccc(F)c(C=Cc3ccc(S(C)(=O)=O)cc3)c2)c2ncccc2c1
Reaction #268128
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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