chromium trioxide

CC1(C)CCC(=O)c2cc(Br)ccc21
Reaction #1309
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2cc(Br)ccc21
Reaction #1463
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1[nH]c2cc(Cl)cc(Cl)c2c(=O)o1
Reaction #3199
title compound
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)c2c(=O)oc(=O)[nH]c2c1
Reaction #3205
title compound
Выход 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1[nH]c2cc(I)ccc2c(=O)o1
Reaction #3215
title compound
Выход 81.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)OC(OC(C)=O)c1ccc(C(OC(C)=O)(C(F)(F)F)C(F)(F)F)cc1
Reaction #4838
α,α -bis-acetyloxy-4-[1-(acetyloxy)-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]toluene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(O)CCOc1cccc(F)c1
Reaction #41973
sub-title compound
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@@H](OC(=O)OCc1ccccc1)[C@H]1C(=O)N[C@@H]1[C@@H](C)C(=O)O
Reaction #49998
(3S,4S)-4-(1-(R)-carboxyethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
[O]=[Cr](=[O])([O-])[F].c1cc[nH+]cc1
Reaction #52042
pyridinium fluorochromate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc2c(c1)C(C)(C)CCC2=O
Reaction #52343
title compound
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1(C)CCC(=O)c2cc(Br)ccc21
Reaction #52845
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCCCCC(C)(C)c1ccc(C2CN(Cc3ccccc3)CCC2=O)c(OCc2ccccc2)c1
Reaction #54345
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=C(O)c1cnn(-c2cccc(C(F)(F)F)c2)c1
Reaction #55558
1-(m-trifluoromethylphenyl)pyrazole-4-carboxylic acid
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
C[C@]12CCCC(=O)[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](OC3CCCCO3)CC[C@@H]12
Reaction #55611
17β-tetrahydropyranyloxy-5α-androstan-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCC(CC(=O)C(N)=O)C(C)[N+](=O)[O-]
Reaction #63858
4-ethyl-5-nitro-2-oxo-hexanamide
Выход 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COC(=O)c1ccc(C(=O)O)cc1
Reaction #64765
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(=O)C1COc2cc(C(C)=O)ccc2O1
Reaction #65435
Ethyl 6-acetyl-2,3-dihydro-1,4-benzodioxin-2-carboxylate
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1cn([C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)CC2=O)c(=O)[nH]c1=O
Reaction #65676
title compound
Выход 59.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(=O)Oc1ccc(COC(=O)NCC=O)cc1
Reaction #67537
aldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCOC(=O)NCC=O
Reaction #67539
aldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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