2-[4-(tert-butyl dimethylsilyloxy)phenyl]acetyl chloride

CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccccc2)cc1
Reaction #324378
Compound 11a
Ausbeute 75.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2/C=C/c2ccccc2)cc1
Reaction #324380
Compound 11b
Ausbeute 69.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=C(c1ccccc1)c1nc(-c2ccc(O[Si](C)(C)C(C)(C)C)cc2)cnc1NC(=O)Cc1ccc(O[Si](C)(C)C(C)(C)C)cc1
Reaction #324382
Compound 11c
Ausbeute 33.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2cccc3ccccc23)cc1
Reaction #324384
Compound 11d
Ausbeute 55.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccc3ccccc3c2)cc1
Reaction #324386
Compound 11e
Ausbeute 58.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2cccs2)cc1
Reaction #324388
Compound 11f
Ausbeute 44.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccsc2)cc1
Reaction #324390
Compound 11g
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2cc3ccccc3s2)cc1
Reaction #324392
Compound 11h
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2csc3ccccc23)cc1
Reaction #324394
Compound 11i
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccc(O[Si](C)(C)C(C)(C)C)cc2)cc1
Reaction #324396
Compound 11j
Ausbeute 81.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2cc3sccc3s2)cc1
Reaction #324398
Compound 11k
Ausbeute 58.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2cc3sc4ccsc4c3s2)cc1
Reaction #324400
Compound 11l
Ausbeute 20.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccc(-c3cccs3)s2)cc1
Reaction #324402
Compound 11m
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CN(C)c1ccc(-c2nc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)cnc2NC(=O)Cc2ccc(O[Si](C)(C)C(C)(C)C)cc2)cc1
Reaction #324404
Compound 11n
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #324406
Compound 11o
Ausbeute 48.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2C#Cc2ccccc2)cc1
Reaction #324408
Compound 11p
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2CCc2ccccc2)cc1
Reaction #324412
Compound 11r
Ausbeute 45.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2cnc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)cn2)cc1
Reaction #324414
Compound 11s
Ausbeute 74.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccccc2)cc1
Reaction #420774
Compound 11a
Ausbeute 75.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2/C=C/c2ccccc2)cc1
Reaction #420776
Compound 11b
Ausbeute 69.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
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