Substructure Search

C=CCCCCCCCCCO

C[C@]12CC[C@H]3[C@@H](CC[C@@H]4CC(=O)CC[C@@H]43)[C@@H]1CC[C@@H]2O
Reaction #7507
title compound
Yield 107.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC=CCCCCCC(=O)O
Reaction #56094
7-dodecenoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC=CCCCCC(=O)O
Reaction #56096
6-undecenoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)C=C[C@@]43C)[C@@H]1C[C@@H](C#N)[C@@H]2C(=O)CO
Reaction #63000
16α-cyano-11β,21-dihydroxy-3,20-dioxo-1,4-pregnadiene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(C=CC1C=CC(=O)C1=CCCCCCC(=O)OC)O[Si](C)(C)C(C)(C)C
Reaction #63769
4-(3-t-butyldimethylsilyloxy-1-octenyl)-5-(6-methoxycarbonylhexylidene)-2-cyclopentenone
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CCCCCCCCC(=O)NCCO)NCCO
Reaction #81530
N,N'-bis-(2-hydroxyethyl)-trans-2-dodecendiamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@H]1[C@H](C)CC2C3CCC4=CC(=O)CC[C@]4(C)C3=CC[C@@]21C
Reaction #86295
desired product
Yield 30.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CC2C3CCC4=CC(=O)C=C[C@]4(C)C3=CC[C@]2(C)[C@H]1C(=O)CO
Reaction #86296
product
Yield 37.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CC2C3CCC4=CC(=O)C=C[C@]4(C)C3=CC[C@]2(C)[C@@]1(O)C(=O)CO
Reaction #86298
(10S,13S,16R,17R)-17-hydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,10,12,13,14,15,16,17-decahydro-3H-cyclopenta[a]phenanthren-3-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CC2C3CCC4=CC(=O)CC[C@]4(C)C3=CC[C@]2(C)[C@@]1(C)C(=O)CO
Reaction #86299
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCC(=O)NCCC=C
Reaction #90836
desired product
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)CBr
Reaction #92981
above-identified compound
Yield 74.6%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
Yield 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(C)=O
Reaction #92985
above-identified compound
Yield 35.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=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 #92986
above-identified compound
Yield 35.4%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
Reaction #92987
above-identified compound
Yield 70.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(=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 #92988
above-identified compound
Yield 77.5%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)CCC(C)C
Reaction #92989
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)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 #92990
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(=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 #92991
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
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