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1366041

O=C(NCC[C@H](OCc1ccccc1)C(=O)O)OCc1ccccc1
Reaction #72436
(S)-2-benzyloxy-4-benzyloxycarbonylaminobutyric acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@@H](OCc1ccccc1)C(=O)O)OCc1ccccc1
Reaction #72437
title compound
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCC(OCc1ccccc1)C(=O)O)OCc1ccccc1
Reaction #255643
DOI: 10.1039/C8SC04228D
O=C(NCCC(OC(=O)c1ccccc1)C(=O)O)OCc1ccccc1
Reaction #389727
DOI: 10.1039/C8SC04228D
O=C(NCCC(OC(=O)c1ccccc1)C(=O)Oc1c(F)c(F)c(F)c(F)c1F)OCc1ccccc1
Reaction #783890
DOI: 10.1039/C8SC04228D
O=C(OCc1ccccc1)Oc1ccccc1[N+](=O)[O-]
Reaction #1654868
DOI: 10.1039/C8SC04228D
O=C(NCCC(OC(=O)c1ccccc1)C(=O)O)OCc1ccccc1
Reaction #1660710
DOI: 10.1039/C8SC04228D
O=C(NCC[C@H](OCc1ccccc1)C(=O)O)OCc1ccccc1
Reaction #1773100
(S)-2-benzyloxy-4-benzyloxycarbonylaminobutyric Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@@H](OCc1ccccc1)C(=O)O)OCc1ccccc1
Reaction #1773101
title compound
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@H](OCc1ccccc1)C(=O)O)OCc1ccccc1
Reaction #1862940
(S)-2-benzyloxy-4-benzyloxycarbonylaminobutyric acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@@H](OCc1ccccc1)C(=O)O)OCc1ccccc1
Reaction #1862941
title compound
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@H](OC(=O)c1ccccc1)C(=O)O)OCc1ccccc1
Reaction #2036791
(S)-2-(benzoyloxy)-4-(benzyloxycarbonylamino)butanoic acid
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@H](OC(=O)c1ccccc1)C(=O)Oc1c(F)c(F)c(F)c(F)c1F)OCc1ccccc1
Reaction #2036792
(S)-4-(benzyloxycarbonylamino)-1-oxo-1-(perfluorophenoxy)butan-2-yl benzoate
Выход 88.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@H](OC(=O)c1ccccc1)C(=O)O)OCc1ccccc1
Reaction #2036793
foam ( 2 )
Выход 64.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@H](OC(=O)c1ccccc1)C(=O)O)OCc1ccccc1
Reaction #2036794
crude intermediate ( 2 )
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[C@H](OC(=O)c1ccccc1)C(=O)O)OCc1ccccc1
Reaction #2036795
crude intermediate ( 2 )
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1O
Reaction #2036796
3′,4′,3′″,4′″-tetra-deoxy-1-(2(S)-hydroxy-3-amino-propionyl)-neomycin
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)Oc1ccccc1[N+](=O)[O-]
Reaction #2036798
( 5 )
Выход 26.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCC(OC(=O)c1ccccc1)C(=O)O)OCc1ccccc1
Reaction #2410656
DOI: 10.1039/C8SC04228D