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CCCCCCCCCCCCC

NC(=O)CCCCCCCCCCC(Cl)(Cl)C(=O)O
Reaction #187880
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCC(CCOC(c1ccccc1)(c1ccc(OC)cc1)c1ccc(OC)cc1)OC(=O)CCC(=O)O
Reaction #193978
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCC2(C)C(=CC(=O)C3C4CCC(=O)C4(C)CCC32)C1
Reaction #198415
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCC(CCP(=O)(OCC)OCC)C(=O)O
Reaction #210662
DOI: 10.1039/C8SC04228D
O=C1CCCCCCCCCCC(O)CCCO1
Reaction #213675
DOI: 10.1039/C8SC04228D
CCOc1cc(C=O)ccc1O
Reaction #215688
ethyl vanillin
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@H](CC(O)C(C(=O)OC)N(Cc1ccccc1)c1ccccc1)O[Si](C)(C)C(C)(C)C
Reaction #216252
methyl (5R)-2-(N-benzylanilino)-5-(t-butyldimethylsiloxy)-3-hydroxyhexadecanoate
Rendimiento 7.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCC(Cl)C(=O)O
Reaction #225348
DOI: 10.1039/C8SC04228D
CCC1(c2ccc(O)cc2)CSc2cc(O)ccc2C1CCCCCCCCC(CCCCCC(F)(F)C(F)(F)F)C(=O)O
Reaction #230062
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCc1ccc2c(C(N)=O)c(OC)ccc2c1
Reaction #230724
DOI: 10.1039/C8SC04228D
C=CCCCCCC(CCCCCC(F)(F)C(F)(F)F)C(=O)OCC
Reaction #235316
DOI: 10.1039/C8SC04228D
CC#CCCC(C)(O)C=CC1C(O)CC(=O)C1CCCCCCC(=O)O
Reaction #239614
DOI: 10.1039/C8SC04228D
CCCCCC(C)(O)C=CC1CCC(=O)C1CCCCCCC(=O)OC
Reaction #247116
DOI: 10.1039/C8SC04228D
CC(=O)OC1CCC2(C)C(=CC(=O)C3C2CCC2(C)C(OC(C)=O)CCC32)C1
Reaction #264473
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCC(CC(N)=O)OS(C)(=O)=O
Reaction #274781
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #280368
DOI: 10.1039/C8SC04228D
O=C(O)CCCCCCC1C(=O)CCC1C=CC(O)CC1CCCCC1
Reaction #290684
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCC1(O)CC(OC)OC1CO
Reaction #298349
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCc1ccc2nc3c(c(Cl)c2c1)CCCC3
Reaction #301151
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #302720
DOI: 10.1039/C8SC04228D
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