t-butylammonium iodide

CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #1475
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #568392
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
O=C(Cn1ccc(OCc2ccccc2)cc1=O)c1ccc2c(c1)CCN(C(=O)C(F)(F)F)CC2
Reaction #651265
4-Benzyloxy-1-{2-oxo-2-[3-(2,2,2-trifluoro-acetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-ethyl}-1H-pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=C(Cn1ccc(OCc2ccccc2)cc1=O)c1ccc2c(c1)CN(C(=O)C(F)(F)F)CC2
Reaction #651384
4-Benzyloxy-1-{2-oxo-2-[2-(2,2,2-trifluoro-acetyl)-1,2,3,4-tetrahydro-isoquinolin-7-yl]-ethyl}-1H-pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
COc1ccc(S(=O)(=O)Oc2cc(OC)c(OC)c(OC)c2)cc1N
Reaction #671110
desired compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
CCOC(=O)C1CC(=O)N(Cc2ccc(OC)cc2)C1C
Reaction #682398
ethyl rac-(2R,3S)-1-(4-methoxybenzyl)-2-methyl-5-oxopyrrolidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #698207
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
CN(C)CC#Cc1ccc(-c2ccc(Cl)cc2)c(CN2CCN(C(=O)OC(C)(C)C)CC2)c1
Reaction #716786
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #722775
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #1051064
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #1052681
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #1079298
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_10
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #1092082
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_04
CN(C)CC#Cc1ccc(-c2ccc(Cl)cc2)c(CN2CCN(C(=O)OC(C)(C)C)CC2)c1
Reaction #1132357
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(S(=O)(=O)Oc2cc(OC)c(OC)c(OC)c2)cc1N
Reaction #1147021
desired compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_02
COCCOc1ccn2c(-c3ccc4cccc(OCCN)c4n3)cnc2c1
Reaction #1182919
desired product
Ausbeute 35.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #1355642
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #1376490
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_05
O=C(OCc1ccccc1)c1cc(OCc2ccccc2)c(OCc2ccccc2)c(OCc2ccccc2)c1
Reaction #1485902
1a
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CN(C)CC#Cc1ccc(-c2ccc(Cl)cc2)c(CN2CCN(C(=O)OC(C)(C)C)CC2)c1
Reaction #1606007
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
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