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401917

COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #46634
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #49131
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H](N)Cc1c[nH]c2ccccc12.Cl
Reaction #53601
H-Trp-OtBu HCl
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #155440
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #167534
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(c1ccccc1)n1c(=O)[nH]c2ccc(Cl)cc21
Reaction #212026
DOI: 10.1039/C8SC04228D
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #325081
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(c1ccccc1)n1c(=O)n(C(=O)OC(C)(C)C)c2ccc(Cl)cc21
Reaction #376414
DOI: 10.1039/C8SC04228D
Cc1cccc(NC(=O)NCC(=O)N(c2ccccc2)C(C(=O)OC(C)(C)C)c2ccccc2Cl)c1
Reaction #385101
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C(N)c1ccc(C(=O)Nc2ccc(Cl)c(-c3ccccn3)c2)c(Cl)c1
Reaction #391738
DOI: 10.1039/C8SC04228D
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #476062
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #505074
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #541135
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #676109
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #690481
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #712699
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(N)c1ccc(C(=O)Nc2ccc(Cl)c(-c3ccccn3)c2)c(Cl)c1
Reaction #720170
2-chloro-N-(4-chloro-3-(pyridin-2-yl)-phenyl)-4-(BOC-aminomethyl)-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](C(=O)OC(C)(C)C)c1ccccc1
Reaction #732577
(R)-tert-butyl 2-(methoxycarbonylamino)-2-phenylacetate
Выход 71.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(N)c1ccc(C(=O)Nc2ccc(Cl)c(-c3ccccn3)c2)c(Cl)c1
Reaction #1010020
2-chloro-N-(4-chloro-3-(pyridin-2-yl)-phenyl)-4-(BOC-aminomethyl)-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H](c1ccccc1)N1CCCCC1
Reaction #1010593
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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