子结构搜索

442882

CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNN=C1CCCC1
Reaction #57463
tert-butyl N-[(1S,2R)-1-benzyl-3-(2-cyclopentylidenhydrazino)-2-hydroxypropyl]carbamate
收率 14.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(O)CNN=C1CCCC1
Reaction #293678
DOI: 10.1039/C8SC04228D
COC(=O)N[C@H](C(=O)NN(Cc1ccc(-c2nnn(C(C)(C)C)n2)cc1)C[C@H](O)[C@@H](N)Cc1ccccc1)C(C)(C)C.Cl
Reaction #467404
1-[4-(2-tert-Butyl-2H-tetrazol-5-yl)-phenyl]-4(S)-hydroxy-5(S)-amino-2-N-[N-methoxycarbonyl-(L)-tert-leucyl]amino-6-phenyl-2-azahexane hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(O)CN(Cc1ccc(-c2ccccn2)cc1)NC(=O)OC(C)(C)C
Reaction #595469
( 7 )
收率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Cl.NC(Cc1ccccc1)C(O)CN(N)Cc1ccc(-c2ccccn2)cc1
Reaction #595470
( 8 )
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(O)CN(Cc1ccc(-c2ccccn2)cc1)NC(=O)OC(C)(C)C
Reaction #601785
( 7 )
收率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Cl.NC(Cc1ccccc1)C(O)CN(N)Cc1ccc(-c2ccccn2)cc1
Reaction #601786
( 8 )
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@H](C(=O)NN(Cc1ccccc1)C[C@H](O)[C@@H](N)Cc1ccccc1)C(C)(C)C
Reaction #730244
title compound
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)OC)C(=O)NN(Cc1ccc(-c2ccccn2)cc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #730245
title compound
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)OC)C(=O)NN(Cc1ccc(-c2ccccn2)cc1)C[C@H](O)[C@@H](N)Cc1ccccc1
Reaction #730246
title compound
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@H](C(=O)NN(Cc1ccc(-c2ccccn2)cc1)C[C@H](O)[C@@H](N)Cc1ccccc1)C(C)C
Reaction #730250
title compound
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@H](C(=O)NNC[C@H](O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(C)(C)C
Reaction #730251
title compound
收率 96.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@H](C(=O)NN(Cc1csc(-c2cc(C)on2)n1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(C)(C)C
Reaction #730252
title compound
收率 99.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)OC)C(=O)NN(Cc1ccccc1)C[C@H](O)[C@@H](N)Cc1ccccc1
Reaction #730254
title compound
收率 91.1%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)OC)C(=O)NN(Cc1ccc(OC)cc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #730255
title compound
收率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(O)CN(Cc1ccc(-c2ccccn2)cc1)NC(=O)OC(C)(C)C
Reaction #765412
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(CN(CC1CCCCC1)NC(=O)OC(C)(C)C)OC(=O)c1ccccn1
Reaction #897984
DOI: 10.1039/C8SC04228D
COC(=O)N[C@H](C(=O)NN(Cc1ccc(-c2nnn(C(C)(C)C)n2)cc1)C[C@H](O)[C@@H](N)Cc1ccccc1)C(C)(C)C.Cl
Reaction #1364181
1-[4-(2-tert-Butyl-2H-tetrazol-5-yl)-phenyl]-4(S)-hydroxy-5(S)-amino-2-N-[N-methoxycarbonyl-(L)-tert-leucyl]amino-6-phenyl-2-azahexane hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(Cc1ccc(-c2ccccc2)cc1)NC(=O)OC(C)(C)C
Reaction #1378960
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](CN(CC1CCCCC1)NC(=O)OC(C)(C)C)OC(=O)c1ccccn1
Reaction #1378978
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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