hexamethylphosphorous triamide

CCCC[C@@H](C)C[C@@H](/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)C(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #3123
methyl(11R,12S,13E,15S,17R)-9-isobutyryloxy-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC[C@@H](/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)c2ccccc2)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #3127
methyl(11R,12S,13E,15S)-9-benzoyloxy-11,15-bis(tert-butyldimethylsiloxy)-7-thiaprosta-8,13-dienoate
Ausbeute 55.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(CCCC(=O)OCc1ccccc1)=C(F)F
Reaction #6564
Benzyl 6,6-difluoro-5-methyl-5-hexenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(CCCCCC(=O)OCc1ccccc1)=C(F)F
Reaction #6568
Benzyl 8,8-difluoro-7-methyl-7-octenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1c(F)cc(C[C@@H]([C@H](OCc2ccccc2)[C@H]2CO[C@@H](OCC(C)(C)C)[C@H](C)N2C(=O)OC(C)(C)C)N(Cc2ccccc2)Cc2ccccc2)cc1F
Reaction #48742
desired compound
Ausbeute 55.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1cc(-c2ccsc2)c2ccc(CCl)cc2o1
Reaction #49853
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(CCCC(=O)OCc1ccccc1)=C(F)F
Reaction #222241
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C1CN2CCCN3CCN(C1)P23
Reaction #235688
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC(Cn1ncc2c(Br)ncnc21)c1ccccc1
Reaction #267249
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cnc(SC)cn1
Reaction #272245
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)CCCC(C)=C(F)F
Reaction #297189
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(C[C@@H]1[C@H](C=C(Cl)Cl)C1(C)C)OC
Reaction #311928
residue
Ausbeute 94.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
COc1cc(C)c(C(=O)c2c(OC)cncc2C(F)(F)F)c(OC)c1OC
Reaction #329616
4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1cc(C)c(C(=O)c2c(OC)cncc2C(F)(F)F)c(OC)c1OC
Reaction #330966
4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CN1CCc2cccc3c2[C@@H]1Cc1ccc(C=O)c(O)c1-3.Cl
Reaction #343726
white solid
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
C1CN2CCN3CCN(CCO1)P23
Reaction #346663
10-oxa-1,4,7-triaza-13-phosphatricyclo[5.5.1.04,13 ]tridecane
Ausbeute 102.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
C1CN2CCN3CCN(C1)P23
Reaction #346664
1,4,7-triaza-11-phosphatricyclo[5.3.1.04,11 ] undecane
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
C1CN2CCCN3CCCN(C1)P23
Reaction #346665
1,5,9-triaza- 13-phosphatricyclo[7.3.1.05,13 ]tridecane
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
C1CN2CCCN3CCN(C1)P23
Reaction #346666
1,4,8-triaza-12-phosphatricyclo[6.3.1.04,12 ]dodecane
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
CN1CCN2CCN(C)P12
Reaction #346667
2,8-dimethyl-2,5,8-triaza-1-phosphabicyclo[3.3.0]octane
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
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