(R)-tetrahydro-1-naphthylamine

c1ccc2c(c1)CCC[C@H]2Nc1nc2ccccc2[nH]1
Reaction #44834
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@@H](C(=O)N[C@H](C(=O)N1C[C@@H](N=[N+]=[N-])C[C@H]1C(=O)N[C@@H]1CCCc2ccccc21)C(C)(C)C)N(C)C(=O)OC(C)(C)C
Reaction #324424
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)N1Cc2cc(O)ccc2C[C@H]1C(=O)N[C@@H]1CCCc2ccccc21
Reaction #426411
title compound
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(C)OC(=O)N1C[C@@H](NC(=O)OCC2c3ccccc3-c3ccccc32)C[C@H]1C(=O)N[C@@H]1CCCc2ccccc21
Reaction #426418
title compound
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C1C[C@@H](C(=O)N[C@@H]2CCCc3ccccc32)N(C(=O)OCc2ccccc2)C1
Reaction #426428
title compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C(N[C@@H]1CCCc2ccccc21)C1=CCOC1
Reaction #426598
(R)—N-(1,2,3,4-tetrahydronaphthalen-1-yl)-2,5-dihydrofuran-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1nocc1C(=O)NC1CCCc2ccccc21
Reaction #426602
title compound
المردود 62.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C(=O)NC(C(=O)N1CCC2C1C(C(=O)NC1CCCc3ccccc31)CN2S(C)(=O)=O)C1CCCCC1)N(C)C(=O)OC(C)(C)C
Reaction #534146
22
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CC(C)(C)OC(=O)N1C[Si](C)(C)C[C@H]1C(=O)N[C@@H]1CCCc2ccccc21
Reaction #614918
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(C)(C)OC(=O)N1C[C@@H](NC(=O)OCC2c3ccccc3-c3ccccc32)C[C@H]1C(=O)N[C@@H]1CCCc2ccccc21
Reaction #614921
title compound
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COC(=O)c1ccc(CO[C@H]2C[C@@H](C(=O)N[C@@H]3CCCc4ccccc43)N(C(=O)OC(C)(C)C)C2)cc1
Reaction #614926
title compound
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Clc1cncc(N[C@@H]2CCCc3ccccc32)n1
Reaction #1331568
product
المردود 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
O=C1c2ccccc2C(=O)N1[C@@H]1CCCc2ccccc21
Reaction #1450400
title compound
المردود 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
O=C1CCN([C@@H]2CCCc3ccccc32)CC1
Reaction #1507856
(R)-1-(1,2,3,4-tetrahydro-naphtalen-1-yl)-piperidine-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_06
O=CN[C@@H]1CCCc2ccccc21
Reaction #1531884
(R)—N-(1,2,3,4-tetrahydronaphthalen-1-yl)formamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
O=C(N[C@@H]1CCCc2ccccc21)C1=CCOC1
Reaction #1540701
(R)—N-(1,2,3,4-tetrahydronaphthalen-1-yl)-2,5-dihydrofuran-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_01
Cc1nocc1C(=O)NC1CCCc2ccccc21
Reaction #1540705
title compound
المردود 62.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_01
—
Reaction #1569092
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
O=C(N[C@@H]1CCCc2ccccc21)C1=CCOC1
Reaction #1731302
(R)—N-(1,2,3,4-tetrahydronaphthalen-1-yl)-2,5-dihydrofuran-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
Cc1nocc1C(=O)NC1CCCc2ccccc21
Reaction #1731306
title compound
المردود 62.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
الصفحة 1التالي