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7175

CCCCOC(=O)COC(C)(C)C
Reaction #4466
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)C(O)CO
Reaction #70102
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2,3-dihydroxypropanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)CO
Reaction #92982
above-identified compound
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)C(C)(C)C
Reaction #92998
above-identified compound
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CCCC(=O)O
Reaction #92999
above-identified compound
Ausbeute 56.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)c1ccccc1
Reaction #93000
above-identified compound
Ausbeute 89.1%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CC1CCCC1
Reaction #93001
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(C)C(=O)OCC(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #93002
above-identified compound
Ausbeute 19.8%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CC(C)=O
Reaction #93004
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CC(C)(C)C
Reaction #93011
above-identified compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)[C@H](CC(C)C)NC(=O)OC(C)(C)C
Reaction #93016
above-identified compound
Ausbeute 80.5%DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC(OC(=O)COc3ccccc3)CC1=CCC1C2CCC2(C)C(=NO)CCC12
Reaction #173001
DOI: 10.1039/C8SC04228D
CCC1CC2C3CCC4=CC(=O)CCC4C3CCC2(C)C1OC(=O)COC(=O)CC(C)(C)C
Reaction #181613
DOI: 10.1039/C8SC04228D
CCCCOC(=O)C(C)Oc1cccc(Oc2ccc(CN(Cc3ccccc3)c3cccc([N+](=O)[O-])c3C)cc2)c1
Reaction #190534
DOI: 10.1039/C8SC04228D
O=C([O-])C(F)(F)F
Reaction #203209
DOI: 10.1039/C8SC04228D
CCC(Oc1ccc(Br)cc1)C(=O)OC1CC(C(C)(C)C)C=C2C=CC(C)C(CCC3CC(C(C)(C)C)C(O[SiH](C)C)C(=O)O3)(O[SiH](C)C)C21
Reaction #211947
DOI: 10.1039/C8SC04228D
CCCCCOC(=O)COc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #212694
DOI: 10.1039/C8SC04228D
CCCCOC(=O)CO[Si](C)(C)C(C)(C)C
Reaction #215692
n-Butyl (t-butyl-dimethyl-silanyloxy)-acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCO[C@@H](CC(C)C)C(=O)O
Reaction #220194
compound 10
Ausbeute 74.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccccc1OC(CC)C(=O)OC1CC(C(C)(C)C)C=C2C=CC(C)C(CCC3CC(C(C)(C)C)C(O[SiH](C)C)C(=O)O3)(O[SiH](C)C)C21
Reaction #222398
DOI: 10.1039/C8SC04228D
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