Teilstruktursuche

CCCC(CC(CC)O)O

CCCCCCC(C(=O)O)C(O)CC(CCCCC)OCc1ccccc1
Reaction #5723
rac-(2RS,3RS,5SR)-5-benzyloxy-2-hexyl-3-hydroxy-decanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC1CC(=O)[C@@H](CCCCCC)C(=O)O1
Reaction #6154
tetrahydro-3-hexyl-4-oxo-(R)-6-undecyl-2H-pyran-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@@H]1C[C@H](O)[C@H](CCCCCC)C(=O)O1
Reaction #6155
(3S,4S,6R)-tetrahydro-3-hexyl-4-hydroxy-6-undecyl-2H-pyran-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@@H]1C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](CCCCCC)C(=O)O1
Reaction #6156
(3S,4S,6R)-tetrahydro-3-hexyl-4-[(t-butyldimethylsilyl)oxy]-6-undecyl-2H-pyran-2-one
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC[C@H](OC(=O)[C@H](C)NC=O)[C@H]1OC(=O)[C@H]1CCCCCC
Reaction #6159
N-formyl-L-alanine (S)-1-[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl)-4-pentenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC[C@@H](C[C@@H]1OC(=O)[C@H]1CCCCCCCCCC)OC(=O)[C@H](CC(C)C)NC=O
Reaction #6161
N-formyl-L-leucine (S)-1-[[(2S,3S)-3-decyl-4-oxo-2-oxetanyl]methyl]-4-pentenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #50189
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(O)C(F)(F)CCC[C@@H]1[C@H]2CC(=O)O[C@H]2C[C@H]1OC1CCCCO1
Reaction #50190
title compound ( 33 )
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(/C=C/[C@@H]1[C@H]2CC(=O)O[C@H]2C[C@H]1OC1CCCCO1)O[Si](C)(C)C(C)(C)C
Reaction #50191
title compound ( 46 )
DOI: 10.6084/m9.figshare.5104873.v1
C1=CCCCCCC2OC2CCCCCC1
Reaction #63431
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/[C@@H]1[C@H]2CC(=O)O[C@H]2C[C@H]1OC(=O)c1ccccc1)CCc1ccccc1
Reaction #96016
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1C(O)CC(O)(C(=O)OCc2ccccc2)OC1C(O)C(O)COC(=O)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #164435
( 1-5 )
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C)OC(CCc1ccccc1)CCC1C(OC(C)OCC)CC2OC(O)CC21
Reaction #183462
DOI: 10.1039/C8SC04228D
CC(CCCC(C)(O)CO)C1CCC2C3C(Br)C=C4CC(O)CC(O)C4(C)C3CCC12C
Reaction #186987
DOI: 10.1039/C8SC04228D
CCOC(C)OC1(C)CCC(O[Si](CC)(CC)CC)CC(=O)OC(C(C)=CC=CC(C)CC2OC2C(C)C(CC)OC(=O)c2ccccc2)C(C)C=CC1O
Reaction #204819
DOI: 10.1039/C8SC04228D
C=CC(=O)NCCSCCCC(=O)C(O)C(OCC(=O)O)C(O)C(O)CO
Reaction #205538
DOI: 10.1039/C8SC04228D
CCCCCC(C=CC1C(OC2CCCCO2)CC2OC(C(Br)CCCC(=O)OC)CC21)OC1CCCCO1
Reaction #213779
DOI: 10.1039/C8SC04228D
CCCCCCCCCCC[C@@H](C[C@@H]1OC(=O)[C@H]1CCCCCC)Oc1ccccc1C(N)=O
Reaction #216250
o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide
Ausbeute 49.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC(O)CC(OC)(C2CSC(=O)N2Cc2ccc(OC)cc2)O1
Reaction #224053
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)CCCC1CCC2C(CC(O)C2C=CC(COc2cc(F)ccc2F)OC2CCCCO2)OC1
Reaction #231024
DOI: 10.1039/C8SC04228D
Seite 1Weiter