بحث البنية الفرعية

1251438

O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #74723
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #74724
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #74878
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #74879
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #311410
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #311411
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCC[C@H](NC(=O)c1cnc(C)nc1)C(=O)N1C[C@H](Oc2nc3ccccc3nc2-c2nc3ccccc3s2)C[C@H]1C(=O)N[C@]1(C(=O)OCC)C[C@H]1C=C
Reaction #325259
(1R,2S)-ethyl 1-((2S,4R)-1-((S)-2-(2-methylpyrimidine-5-carboxamido)non-8-enoyl)-4-(3-(benzo[d]thiazol-2-yl)quinoxalin-2-yloxy)pyrrolidine-2-carboxamido)-2-vinylcyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCC[C@H](NC(=O)c1cnc(C)cn1)C(=O)N1C[C@H](Oc2nc3ccccc3c3ccccc23)C[C@H]1C(=O)N[C@]1(C(=O)OCC)C[C@H]1C=C
Reaction #325262
(1R,2S)-ethyl 1-((2S,4R)-1-((S)-2-(5-methylpyrazine-2-carboxamido)non-8-enoyl)-4-(phenanthridin-6-yloxy)pyrrolidine-2-carboxamido)-2-vinylcyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C[C@H](O)[C@H](CC(C)C)NC(=O)OC(C)(C)C
Reaction #342800
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #350131
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #350132
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
NCC(O)CCC(NC(=O)OCc1ccccc1)C(=O)O
Reaction #409008
DOI: 10.1039/C8SC04228D
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #459595
N,N'-dicyclohexylurea
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #459596
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)c2ccc(NC(=N)N)cc2)C(=O)N2CCN(CC(=O)O)C(=O)[C@@H]2CCCNC(=O)c2ccc(NC(=N)N)cc2)cc1.Cl
Reaction #463731
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOC(=O)NCCC(=O)N[C@@H](Cc1c[nH]cn1)C(=O)O
Reaction #499141
white crystalline product
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](CO)NC(=O)[C@H](Cc1c[nH]cn1)N(C(=O)[C@H](Cc1cccc2ccccc12)NC(=O)OCc1ccccc1)C(=O)[C@@H](N)Cc1cccc2ccccc12
Reaction #552087
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)OC(C)(C)C)C(=O)NCC(=O)OCc1ccccc1
Reaction #554536
Boc-D-Ala-Gly-OBzl
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CSC[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc2ccccc2)C(=O)NCCC(=O)O)cc1
Reaction #554538
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=N)NCCC[C@@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc2ccc(OCc3ccccc3)cc2)C(=O)OCc2ccccc2)cc1
Reaction #554539
desired product
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي