N-[bis(dimethylamino)phosphoryl]-N-methylmethanamine

C=Cc1ccccc1CC(N=C(SC)SC)C(=O)N1C2CC3CCC2(CS1(=O)=O)C3(C)C
Reaction #2806
title compound
収率 43.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)C(O)(CC(=O)OC(C)(C)C)c1nccn1COCc1ccccc1
Reaction #3240
title compound
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C=CC1=C(C)CCCC1(C)C)=CC=CC(C)=CC=C(C)CSc1ccccc1
Reaction #3994
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCC[C@H](O[C@@H](Cc1ccccc1)C(=O)OC(c1ccccc1)c1ccccc1)c1ccco1
Reaction #5658
(2S,4S) Benzhydryl 2-Benzyl-4-(2-furyl)-3-oxaoctanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCC[C@H](O[C@H](Cc1ccccc1)C(=O)OC(c1ccccc1)c1ccccc1)c1ccco1
Reaction #5659
(2R,4S) benzhydryl 2-Benzyl-4-(2-furyl)-3-oxaoctanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)CCC=C(C)CCC=C(C)CO[Si](C)(C)C(C)(C)C
Reaction #5753
6,10-dimethyl-11-(dimethyl t-butylsilyl)oxy-5,9-undecadien-2-one
収率 70.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#Cc1ccc(-c2ccc(S)cc2)cc1
Reaction #6111
pale yellow solid
収率 106.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#Cc1ccc(S)c(C#N)c1
Reaction #6115
expected product
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
—
Reaction #6313
SiO2
収率 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)OC(=O)N1CCC(CCO[Si](C)(C)C(C)(C)C)(C(=O)CC(O)Cc2ccccc2)CC1
Reaction #8867
tert-Butyl 4-(4-phenyl-3-hydroxy-1-oxobut-1-yl)-4-(2-(tert-butyldimethylsilyloxy)eth-1-yl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C1CCCCC1
Reaction #9360
cyclohexanecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C1CC(CCOCc2ccccc2)CCC1=O
Reaction #9390
5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #42256
solid
収率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #42262
solid
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=Cc1ccc(CCC(=O)CC(C)=O)cc1
Reaction #44323
6-(4-vinylphenyl)-2,4-hexanedione
収率 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)CC(=O)CCc1ccc(OCc2ccccc2)cc1
Reaction #44324
6-(4-benzyloxyphenyl)-2,4-hexanedione
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #45528
solid
収率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #45534
solid
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCC[C@@]1(C(=O)OC)CO[C@H](C(C)(C)C)N1C=O
Reaction #48542
title compound
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #50478
impure material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
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