2-chlorotrityl chloride resin

CC(C)(C(=O)O)C(=O)NCCCc1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1
Reaction #327483
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C(=O)O)C(=O)NCc1ccccn1
Reaction #327484
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)NCC[C@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O
Reaction #417959
Fmoc-Dab(Boc)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C1Cc2ccccc2N1c1ncc[nH]1
Reaction #500909
Imidazolyl Indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
O=C1Cc2ccccc2N1c1ncc[nH]1
Reaction #516724
Imidazolyl Indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CC(C)(C)OC(=O)NCC[C@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O
Reaction #610704
Fmoc-Dab(Boc)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(C)(C)OC(=O)NCC[C@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O
Reaction #634467
Fmoc-Dab(Boc)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
O=c1ccn(C2CC(O)C(CNC(c3ccccc3)(c3ccccc3)c3ccccc3Cl)O2)c(=O)[nH]1
Reaction #767578
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCN(C)C(=O)c1cncc(C(=O)O)c1
Reaction #819770
title compound
수율 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
C[C@@]1(Cc2ccc(C#N)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(C(=O)N[C@H](CC(N)=O)C(=O)O)n21
Reaction #1127738
(R)-2-{[(R)-5-(4-cyano-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carbonyl]-amino}-succinamic acid
수율 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CCCN(C)C(=O)c1cncc(C(=O)O)c1
Reaction #1232509
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Clc1ccccc1C(c1ccccc1)(c1ccccc1)n1cc[n+](C(c2ccccc2)c2ccc(-c3ccccc3)cc2)c1.[Cl-]
Reaction #1476241
1-[α-(4-biphenylyl)-benzyl]-3-(2-chlorophenyl-diphenyl-methyl)-imidazolium chloride
수율 83.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_01
C=C(CCC(=O)O)c1ccc(C[C@H](NC(=O)OCC2c3ccccc3-c3ccccc32)C(=O)N2CCCCC2)cc1.Clc1ccccc1C(Cl)(c1ccccc1)c1ccccc1
Reaction #1569424
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
C=C(CCC(=O)O)c1cccc(C[C@H](NC(=O)OCC2c3ccccc3-c3ccccc32)C(=O)N2CCCCC2)c1.Clc1ccccc1C(Cl)(c1ccccc1)c1ccccc1
Reaction #1569426
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
Clc1ccccc1C(Cl)(c1ccccc1)c1ccccc1.O=C(O)CCCCCc1ccc(C[C@H](NC(=O)OCC2c3ccccc3-c3ccccc32)C(=O)N2CCCCC2)cc1
Reaction #1569431
title compound
수율 223.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
Clc1ccccc1C(Cl)(c1ccccc1)c1ccccc1.O=C(O)CCCCc1cccc(C[C@H](NC(=O)OCC2c3ccccc3-c3ccccc32)C(=O)N2CCCCC2)c1
Reaction #1569436
title compound
수율 250.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
C=CCCC(=O)N(C)[C@@H](COC(C)(C)C)C(=O)O
Reaction #1569566
(S)-3-(tert-butoxy)-2-(N-methylpent-4-enamido)propanoic acid
수율 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
O=c1ccn([C@H]2C[C@H](O)[C@@H](CNC(c3ccccc3)(c3ccccc3)c3ccccc3Cl)O2)c(=O)[nH]1
Reaction #1905851
title compound
수율 16.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
O=C(N[C@@H](CC1CCCCC1)C(=O)O)OCC1c2ccccc2-c2ccccc21
Reaction #1922746
Fmoc-Cha
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_08
CN[C@H](Cc1ccccc1)C(=O)N[C@H](Cc1ccc(Cl)cc1)C(=O)O
Reaction #1922747
H-NMe(D)Phe-(D)Phe(4-Cl)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_08
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