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C=CCCCCCC

CC[NH+](C(C)C)C(C)C
Reaction #52568
ethyldiisopropyl-ammonium
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)OC2=CC(=O)C3CCC2C3)c(Cl)c1Cl
Reaction #52573
2,3-Dichloro-4-methanesulfonylbenzoic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCC1(C2=CCCC(C)(C)C2)OCCO1
Reaction #54161
1-(3,3-dimethyl-cyclohex-6-en-1-yl)-1,1-ethylenedioxy-pent-4-ene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56547
beta-carotene
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56548
beta-carotene
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56549
beta-carotene
Выход 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56550
beta-carotene
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56554
beta-carotene
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56555
beta-carotene
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C\C=C\C(C)=C\C(=O)O)C(C)(C)CCC1
Reaction #71591
9-(Z)-retinoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C1CCCCCC=C1Br
Reaction #74254
17
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)C1C#CCCCCC1
Reaction #74255
cyclooct-1-yn-3-glycolic acid
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C(=O)CC(C)O)C(C)(C)CC=C1
Reaction #74867
residue
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75275
3,3-dimethyl-1-(2-methyllyl-5-methyl-4-pentenoyl)cyclohexane
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1CCCC(C)(C)C1
Reaction #75276
1-acetyl-3,3-dimethylcyclohexane
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1CCCC(C)(C)C1
Reaction #75277
1-acetyl-3,3-dimethylcyclohexane
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)[C@H](CC1CCNC1=O)NC(=O)OC(C)(C)C
Reaction #87106
tert-butyl ((2S)-4-methyl-3-oxo-1-(2-oxopyrrolidin-3-yl)pent-4-en-2-yl)carbamate
Выход 42.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CC1CCNC1=O)C(=O)[C@@]1(C)CO1
Reaction #87107
tert-butyl ((S)-1-((R)-2-methyloxiran-2-yl)-1-oxo-3-(-2-oxopyrrolidin-3-yl) propan-2-yl)carbamate
Выход 45.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(O)CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162189
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1CCC(C2CCC(C=Cc3cc4ccc(OCC)c(F)c4c(F)c3F)CC2)CC1
Reaction #183042
DOI: 10.1039/C8SC04228D
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