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1142395

CS(=O)(=O)OCC1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #258822
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCC1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #381388
DOI: 10.1039/C8SC04228D
CS(=O)(=O)OC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #428318
(5R)-methanesulfonic acid 3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C[C@@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #428319
(5R)-2-[3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-isoindole-1,3-dione
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #543966
desired product
Ausbeute 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #546190
desired product
Ausbeute 98.4%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #546191
title compound
Ausbeute 88.7%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #834396
Methanesulfonic acid (5R)-3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1)c1ccon1
Reaction #834397
title compound
Ausbeute 57.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(CC1CN(c2ccc(I)c(F)c2)C(=O)O1)c1ccon1
Reaction #888953
DOI: 10.1039/C8SC04228D
CS(=O)(=O)OC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #1334662
(5R)-methanesulfonic acid 3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C[C@@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #1334663
(5R)-2-[3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-isoindole-1,3-dione
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #2036373
(5R)-methanesulfonic acid 3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #2036376
(5R)-methanesulfonic acid 3-(3-fluoro-4-iodophenyl)-2-oxo-oxazolidin-5-ylmethyl ester
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #2036377
(5R)-5-azidomethyl-3-(3-fluoro-4-iodophenyl)-oxazolidin-2-one
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #2036382
(5R)-methanesulfonic acid 3-(3-fluoro-4-iodophenyl)-2-oxo-oxazolidin-5-ylmethyl ester
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #2036383
(5R)-5-azidomethyl-3-(3-fluoro-4-iodophenyl)-oxazolidin-2-one
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #2277865
(5R)-methanesulfonic acid 3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C[C@@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #2277866
(5R)-2-[3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-isoindole-1,3-dione
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1
Reaction #2294623
(5R)-methanesulfonic acid 3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
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