phenacyl bromide

CCn1ncc(C(=O)c2ccc3c(c2C)C(=NOC)CCS3(=O)=O)c1OCC(=O)c1ccccc1
Reaction #1163
4-methoxyimino-5-methyl-6-(1-ethyl-5-phenacyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc2c(c1)ccn1cccc21
Reaction #1269
pyrrolo[2,1-a]isoquinoline
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CBr)c1ccccc1
Reaction #7192
title compound
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(CN1CCN(C(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)[C@H](Cc2c[nH]c3ccccc23)C1)c1ccccc1
Reaction #10264
(2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(1H-indol-3-ylmethyl)-4-(2-phenyl-2-ethanon-1-yl)piperazine
Выход 85.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)CC1CCCC(CC(=O)c2ccccc2)C1=O
Reaction #40886
title compound
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc2c(Nc3nc(-c4ccccc4)cs3)cnc(CNC(=O)OC(C)(C)C)c2cc1OC
Reaction #42945
[6,7-dimethoxy-4-(4-phenyl-thiazol-2-ylamino)isoquinolin-1-ylmethyl]carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCc1nc(-c2ccc(OC3CCN(C)CC3)cc2)cn1-c1ccc(Oc2ccc(F)c(C(F)(F)F)c2)cc1
Reaction #45934
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(CBr)c1ccccc1
Reaction #46478
Intermediate B
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(CBr)c1ccccc1
Reaction #46483
α-bromoacetophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(C[S+]1CCCC1)c1ccccc1.[Br-]
Reaction #53242
phenacyltetrahydrothiophenium bromide
Выход 94.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)OC(=O)N1CCCCC1CC(=O)OCC(=O)c1ccccc1
Reaction #58451
title compound
Выход 74.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)N1CCCCC1CC(=O)OCC(=O)c1ccccc1
Reaction #58456
title compound
Выход 95.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CC1CCCCN1C(=O)OCc1ccccc1)OCC(=O)c1ccccc1
Reaction #58457
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(C[C@@H]1CCCN1C(=O)OCc1ccccc1)OCC(=O)c1ccccc1
Reaction #58469
title compound
Выход 48.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(COc1cc(OCc2ccccc2)ccc1OCc1ccccc1)c1ccccc1
Reaction #59492
2-[2,5-Bis(benzyloxy)phenoxy]-1-phenylethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCCc1nn(CC(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #64497
desired compound
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC1(C)Oc2ccc([N+](=O)[O-])cc2N(CC(=O)c2ccccc2)C1=O
Reaction #65401
3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-4-phenacyl-2H-1,4-benzoxazine
Выход 66.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOc1ccc(-c2nc(-c3ccccc3)co2)cc1OCC
Reaction #69403
product
Выход 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN(CC(=O)c1ccccc1)Cc1ccc(Cl)cc1Cl
Reaction #73934
title compound
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(Cc1ccccc1)N[C@@H]1C(=O)N[C@@H]1SCC(=O)c1ccccc1
Reaction #74883
(3R,4R)-3-phenylacetamido-4-phenacylthioazetidin-2-one
Выход 80.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
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