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217708

CCC1=C[C@H]2[C@@H](C1)C[C@@]2(CN)CC(=O)O
Reaction #638806
powder
Ausbeute 43.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@]1(CNC(=O)OC(C)(C)C)C[C@@H]2CC(CO)=C[C@@H]21
Reaction #638855
Tert-butyl(±)-[(1R,5R,6R)-6-{[(tert-butoxycarbonyl)amino]methyl}-3-(hydroxymethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetate
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C)[C@H]2[C@@H](C1)C[C@@]2(CN)CC(=O)O.Cc1ccc(S(=O)(=O)O)cc1
Reaction #638863
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C[C@@H]2[C@H](C1)C[C@]2(CN)CC(=O)O
Reaction #638864
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C[C@H]2[C@@H](C1)C[C@@]2(CN)CC(=O)O.O=S(=O)(O)c1ccccc1
Reaction #638867
solid
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@@]1(CNC(=O)OC(C)(C)C)C[C@H]2CC(CCF)=C[C@H]21
Reaction #638873
Tert-butyl[(1R,5S,6S)-6-(tert-butoxycarbonylamino)methyl-3-(2-fluoroethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C[C@@H]2[C@H](C1)C[C@]2(CN)CC(=O)OC(C)(C)C
Reaction #638877
Tert-butyl[(1R,5S,6S)-6-aminomethyl-3-ethylbicyclo[3.2.0]hept-3-en-6-yl]acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C[C@H]2[C@@H](C1)C[C@]2(CC(=O)O)CN(C)C(=O)OC(C)(C)C
Reaction #638887
[(1S,5R,6R)-6-{[(tert-butoxycarbonyl)(methyl)amino]methyl}-3-ethylbicyclo[3.2.0]hept-3-en-6-yl]acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCC1=CC2C(C1)CC2(CC(=O)O)CN(C)C(=O)OC(C)(C)C
Reaction #1213086
DOI: 10.1039/C8SC04228D
CCC1=CC2C(C1)CC2(CN)CC(=O)OC(C)(C)C
Reaction #1312495
DOI: 10.1039/C8SC04228D
CCC1=CC2C(C1)CC2(CC(=O)OC(C)(C)C)C[N+](=O)[O-]
Reaction #1587323
Tert-butyl [3-ethyl-6-(nitromethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCC1=CC2C(C1)CC2(CN)CC(=O)O
Reaction #1587324
powder
Ausbeute 43.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C[C@@H]2[C@H](C1)C[C@]2(CN)CC(=O)OC(C)(C)C.O=C(O)[C@H](O)c1ccccc1
Reaction #1587325
tert-butyl [(1R,5S,6S)-6-aminomethyl-3-ethylbicyclo[3.2.0]hept-3-en-6-yl]acetate D-mandelate
Ausbeute 29.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=CC2C(C1)CC2(CC(=O)OC(C)(C)C)C[N+](=O)[O-]
Reaction #1839136
Tert-butyl [3-ethyl-6-(nitromethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCC1=CC2C(C1)CC2(CN)CC(=O)O
Reaction #1839137
powder
Ausbeute 43.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C[C@@H]2[C@H](C1)C[C@]2(CN)CC(=O)OC(C)(C)C.O=C(O)[C@H](O)c1ccccc1
Reaction #1839138
tert-butyl [(1R,5S,6S)-6-aminomethyl-3-ethylbicyclo[3.2.0]hept-3-en-6-yl]acetate D-mandelate
Ausbeute 29.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC2C(C1)CC2(CN)CC(=O)O
Reaction #2223406
DOI: 10.1039/C8SC04228D
CCC1=CC2C(C1)CC2(CN)CC(=O)O
Reaction #2278174
powder
Ausbeute 43.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=CC2C(C1)CC2(CN)CC(=O)O.Cc1ccc(S(=O)(=O)O)cc1
Reaction #2278175
powder
Ausbeute 59.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=CC2C(C1)CC2(CN)CC(=O)OC(C)(C)C
Reaction #2278176
Tert-butyl [6-aminomethyl-3-ethylbicyclo[3.2.0]hept-3-en-6-yl]acetate
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
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