DMPU

Cc1ccc(O)c(C=O)c1
Reaction #1833
product
Выход 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCC#CCCCOC1CCCCO1
Reaction #2037
title compound ( 15 )
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COCCOCOc1ccc(I)cc1CO
Reaction #2853
title compound
Выход 80.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1OCCCCC1Cc1ccccc1
Reaction #3065
2-benzylcaprolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)CCSC(C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1)c1ccccc1
Reaction #3688
beige solid
Выход 93.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C(C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1)c1ccccc1
Reaction #3689
beige solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CN1CCOCC1)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #3693
colorless gum
Выход 106.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Cn1cncn1)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #3706
desired product
Выход 64.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(COc1ccccc1)OCC
Reaction #6531
2-phenoxyacetaldehyde diethyl acetal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1nccn1-c1ccc(N2C[C@H](CO)OC2=O)cc1F
Reaction #8250
title compound
Выход 44.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cn(-c2ccc(N3C[C@H](CO)OC3=O)cc2F)cn1
Reaction #8254
title product
Выход 33.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1c(C)cccc1CO[C@H]1CCC[C@@H](O)C1
Reaction #10479
desired compound
Выход 13.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C1CC2CCCC(C1)C2N1CC(COc2ccc(C#N)cn2)C(C)(C)C1=O
Reaction #44500
titled product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)Cn1ccccc1=O
Reaction #47094
product 425
Выход 76.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H]([C@H](O)c1ccccc1)N(C)C(=O)[C@H](C[C@H]1CCC2(C1)O[C@@H](c1ccccc1)[C@H](c1ccccc1)O2)c1ccc(SC2CC2)cc1
Reaction #48245
2(R)-(4-cyclopropylsulfanylphenyl)-3-(2(S),3(S)-diphenyl-1,4-dioxaspiro[4.4]non-7(R)-yl)-N-(2(R)-hydroxy-1(R)-methyl-2-phenylethyl)-N-methylpropionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1(SCc2ccc(OC)cc2)CC1
Reaction #50794
1-(carboethoxy)-1-(4-methoxybenzylthio)cyclopropane
Выход 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCOC(=O)C1(SCc2ccc(OC)cc2)CCCCC1
Reaction #50796
1-(carboethoxy)-1-(4-methoxybenzylthio)cyclohexane
Выход 56.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(C)(C)OC(=O)CCC(=O)c1c(F)cccc1F
Reaction #53289
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](C#CCCCOC2CCCCO2)CC1
Reaction #53858
trans-Methyl-{4-[5-(tetrahydro-pyran-2-yloxy)-pent-1-ynyl]-cyclohexyl}-carbamic acid tert-butyl ester
Выход 42.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](C#CCCOC2CCCCO2)CC1
Reaction #53921
trans-Methyl-{4-[4-(tetrahydro-pyran-2-yloxy)-but-1-ynyl]-cyclohexyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
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