CAS No.31823-43-5,3-nonenal,(Z)-3-nonenal Suppliers

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3-Nonenal, (3Z)-Appearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damaging the packages. Protect them from

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Synthetic route

: 120018-49-7
(Z)-3-nonenal diisopropyl acetal

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In tetrahydrofuran for 0.333333h; Heating;	99%
With toluene-4-sulfonic acid In tetrahydrofuran for 0.3h; Heating;
With toluene-4-sulfonic acid In tetrahydrofuran; water for 0.166667h; Heating;
With toluene-4-sulfonic acid In tetrahydrofuran; water for 0.25h; Heating;
With toluene-4-sulfonic acid In tetrahydrofuran Heating;

: 10340-23-5
(Z)-non-3-en-1-ol

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
With Dess-Martin periodane In dichloromethane at 20℃; for 1h; Dess-Martin oxidation;	98%
With Dess-Martin periodane In dichloromethane at 0 - 20℃;	97%
With Dess-Martin periodane In dichloromethane at 0 - 20℃; Inert atmosphere;	96%

: 89616-41-1
(2RS,4Z)-4-decen-1,2-diol

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
With lead(IV) acetate; sodium carbonate In dichloromethane at -40 - -30℃; for 0.333333h; Oxidation;	98%
With lead(IV) acetate In dichloromethane at -65℃; for 1.5h;
With lead(IV) acetate In dichloromethane 1.) -20 deg C, 15 min, 2.) -20 -> 0 deg C, 15 min;

: 103229-70-5
1,1-dimethoxy-non-3c-ene

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
With trifluoroacetic acid In chloroform for 1.5h;	94.5%
With acetic acid for 10h; Ambient temperature;	70%
With oxalic acid; benzene-1,2-diol In water; acetone at 45 - 50℃;
With trifluoroacetic acid In chloroform
With water; trifluoroacetic acid In chloroform for 1h;

: 89682-47-3
(3Z)-3-nonenal diethyl acetal

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
With oxalic acid In water; acetone at 60℃; for 1h;	93%
With water; oxalic acid In acetone for 1h; Heating;
With 2,5-bis(1,1-dimethylethyl)-1,4-benzenediol; oxalic acid In water; acetone for 2h; Heating; Yield given;
With formic acid In pentane at -40 - 20℃;

: 77953-94-7
1,1-ethylenedioxy-non-3(Z)-ene

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
With pyridinium p-toluenesulfonate In acetone for 24h; Ambient temperature;	90%
With acetic acid for 24h; Ambient temperature;	82%

: 5502-91-0, 7324-20-1, 26911-36-4, 28396-96-5, 39692-45-0, 63121-49-3, 65941-74-4, 67597-24-4, 90760-93-3, 100018-30-2, 104759-96-8, 122046-44-0, 123410-63-9, 29774-12-7
9(S)-hydroperoxyoctadeca-10Z,12E-dienoic acid

A: 2553-17-5
azelaic acid semialdehyde

B: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
With Cs-9/13-hydroperoxidelyase In aq. phosphate buffer pH=6; Enzymatic reaction;	A 73% B n/a

: 10340-23-5
(Z)-non-3-en-1-ol

A: 2463-53-8, 18829-56-6, 60784-31-8
non-2-enal

B: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
With pyridinium chlorochromate In dichloromethane for 1h; Ambient temperature;	A 5% B 65.4%

: 10340-23-5
(Z)-non-3-en-1-ol

A: 18829-56-6
(E)-2-Nonenal

B: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Swern oxidation;

: 628-71-7
1-Heptyne

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 63 percent / n-BuLi; HMPA / tetrahydrofuran; hexane / 2 h / Heating 2: 83 percent / quinoline; H2 / Lindlar catalyst / ethanol / 2 h 3: HCOOH / pentane / -40 - 20 °C View Scheme
Multi-step reaction with 3 steps 1: 53 percent / n-BuLi / tetrahydrofuran; hexamethylphosphoric acid triamide / 1.) 0 deg C, 4 h; 2.) 27 deg C, 40 h 2: 83 percent / hydrogen / Pd/BaSO4 / methanol / 30 h 3: 93 percent / oxalic acid / acetone; H2O / 1 h / 60 °C View Scheme
Multi-step reaction with 3 steps 1: 1) n-butyllithium / 1) THF, hexane, -5 deg C, 1 h, 2) HMPT, a) -5 deg C, 2 h, b) 20 deg C, 18 h 2: 82 percent / NaBH4, H2, Ni(OAc)2 * 4 H2O / ethanol 3: 94.5 percent / 50percent aq. TFA / CHCl3 / 1.5 h View Scheme

: 90290-02-1
3-nonynal diethyl acetal

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 83 percent / quinoline; H2 / Lindlar catalyst / ethanol / 2 h 2: HCOOH / pentane / -40 - 20 °C View Scheme
Multi-step reaction with 2 steps 1: 83 percent / hydrogen / Pd/BaSO4 / methanol / 30 h 2: 93 percent / oxalic acid / acetone; H2O / 1 h / 60 °C View Scheme
Multi-step reaction with 2 steps 1: 81 percent / i-BuMgBr / Cp2TiCl2 / diethyl ether / 12 h / 26 - 28 °C 2: oxalic acid, 2,5-di-tert-butylhydroquinone / acetone; H2O / 2 h / Heating View Scheme
Multi-step reaction with 2 steps 1: 77 percent / nickel(II) acetate, NaBH4, H2, ethylenediamine / ethanol 2: oxalic acid dihydrate, water / acetone / 1 h / Heating View Scheme

: 66-25-1
hexanal

hydrazine hydrochloride: hydrazine hydrochloride

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: NaN(SiMe3)2 / tetrahydrofuran / -80 °C 2: TsOH / tetrahydrofuran / Heating View Scheme

: 31333-13-8
3-nonyn-1-ol

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 87 percent / H2, quinoline / Lindlar's catalyst / hexane 2: 50.7 percent / pyridinum chlorochromate / CH2Cl2 / 4 h / 0 °C View Scheme
Multi-step reaction with 2 steps 1: H2, quinoline / Pd/BaSO4 / methanol 2: NCS, Me2S / toluene View Scheme
Multi-step reaction with 2 steps 1: 99 percent / hydrogen, pyridine / Pd/BaSO4 / methanol 2: 50 percent / CrO3(Py)2 / L.H. Sarett, J. Chem. Soc., 35, 4000 (1970) View Scheme

: 110-53-2
1-Bromopentane

silver fluoride: silver fluoride

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 61 percent / lithium amide / liquid ammonia; tetrahydrofuran / 3 h 2: 87 percent / H2, quinoline / Lindlar's catalyst / hexane 3: 50.7 percent / pyridinum chlorochromate / CH2Cl2 / 4 h / 0 °C View Scheme

: 66-25-1
hexanal

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 100 percent / NaN(SiMe3)2 / tetrahydrofuran / 12 h / -100 deg C to RT 2: p-TsOH / H2O; tetrahydrofuran / 0.17 h / Heating View Scheme

: 24948-66-1
1-allyl-2-pentylacetylene

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 2.) hydrogen, triethylamine / 2.) Lindlar catalyst / 2.) THF, 23 deg C, 1 atm, 4.5 h 2: lead tetracetate / CH2Cl2 / 1.) -20 deg C, 15 min, 2.) -20 -> 0 deg C, 15 min View Scheme

: 87745-62-8
1,1-dimethoxy-non-3-yne

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 82 percent / NaBH4, H2, Ni(OAc)2 * 4 H2O / ethanol 2: 94.5 percent / 50percent aq. TFA / CHCl3 / 1.5 h View Scheme
Multi-step reaction with 2 steps 1: 82 percent / hydrogen / P-2 Ni / ethanol 2: trifluoroacetic acid, water / CHCl3 / 1 h View Scheme
Multi-step reaction with 2 steps 1: 82 percent / NaBH4 / nickel acetate tetrahydrate / aq. ethanol 2: 50percent aq. TFA / CHCl3 View Scheme
Multi-step reaction with 2 steps 1: H2 / Lindlar catalyst / hexane 2: oxalic acid, benzene-1,2-diol / acetone; H2O / 45 - 50 °C View Scheme

: 42017-07-2
1-heptynyllithium

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 70 percent / HMPT / tetrahydrofuran / -5 °C 2: 82 percent / hydrogen / P-2 Ni / ethanol 3: trifluoroacetic acid, water / CHCl3 / 1 h View Scheme

: 66-25-1
hexanal

magnesium aluminium-isopropylate: magnesium aluminium-isopropylate

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 1.) NaN(SiMe3)2 / 1.) THF, toluene, RT, 1 h, 2.) from -100 to 0 deg C, 4 h 2: 0.1 M aq. p-toluenesulfonic acid / tetrahydrofuran / 0.3 h / Heating View Scheme

: 26001-58-1
(Z)-oct-2-en-1-ol

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 70 percent / pyridinium chlorochromate / CH2Cl2 / 2 h / Ambient temperature 2: 70 percent / dimethylsulfoxide / 1. cooling, 2h 2. room temperature, 12h 3. 50 deg C, 3h 3: 75 percent / PTS / benzene / 6 h / Heating; in a Dean and Stark water seperator 4: 90 percent / PTS / acetone / 24 h / Ambient temperature View Scheme

: 20739-58-6
2-octyn-1-ol

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: 95 percent / H2 / Lindlars'catalyst / hexane 2: 70 percent / pyridinium chlorochromate / CH2Cl2 / 2 h / Ambient temperature 3: 70 percent / dimethylsulfoxide / 1. cooling, 2h 2. room temperature, 12h 3. 50 deg C, 3h 4: 75 percent / PTS / benzene / 6 h / Heating; in a Dean and Stark water seperator 5: 90 percent / PTS / acetone / 24 h / Ambient temperature View Scheme

Yield

Multi-step reaction with 5 steps
1: 95 percent / H2 / Lindlars'catalyst / hexane
2: 70 percent / pyridinium chlorochromate / CH2Cl2 / 2 h / Ambient temperature
3: 70 percent / dimethylsulfoxide / 1. cooling, 2h 2. room temperature, 12h 3. 50 deg C, 3h
4: 75 percent / PTS / benzene / 6 h / Heating; in a Dean and Stark water seperator
5: 90 percent / PTS / acetone / 24 h / Ambient temperature
View Scheme

: 20664-46-4
cis-2-octene oxide

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 70 percent / dimethylsulfoxide / 1. cooling, 2h 2. room temperature, 12h 3. 50 deg C, 3h 2: 75 percent / PTS / benzene / 6 h / Heating; in a Dean and Stark water seperator 3: 90 percent / PTS / acetone / 24 h / Ambient temperature View Scheme

: 77953-93-6, 77953-95-8
1-methoxy-nona-1,3(Z)-diene

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 75 percent / PTS / benzene / 6 h / Heating; in a Dean and Stark water seperator 2: 90 percent / PTS / acetone / 24 h / Ambient temperature View Scheme

: 4450-76-4
1-pentyl tosylate

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: (i) EtMgBr, THF, CH2Cl2, (ii) /BRN= 1879859/ 2: NaOMe / 24 h / 110 - 115 °C 3: H2 / Lindlar catalyst / hexane 4: oxalic acid, benzene-1,2-diol / acetone; H2O / 45 - 50 °C View Scheme

: 91819-64-6
1c-methoxy-non-1-en-3-yne

: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: NaOMe / 24 h / 110 - 115 °C 2: H2 / Lindlar catalyst / hexane 3: oxalic acid, benzene-1,2-diol / acetone; H2O / 45 - 50 °C View Scheme

: 60-33-3
linoleic acid

A: 2553-17-5
azelaic acid semialdehyde

B: 31823-43-5
(Z)-3-nonenal

Conditions

Conditions	Yield
With Cs-9/13-hydroperoxidelyase; St-lipoxygenase1 In aq. phosphate buffer pH=6; Enzymatic reaction;

: 31823-43-5
(Z)-3-nonenal

: 70277-75-7
lithium acetylide

: 129030-85-9
(+/-)-(5Z)-5-undecen-1-yn-3-ol

Conditions

Conditions	Yield
In tetrahydrofuran at -78℃; for 1h;	95%
In tetrahydrofuran for 1h; -78 to 20 deg C; Yield given;

: 31823-43-5
(Z)-3-nonenal

: 1066-54-2
trimethylsilylacetylene

: 118789-62-1
(E/Z)-1-trimethylsilylundec-5-en-1-yn-3-ol

Conditions

Conditions	Yield
Stage #1: trimethylsilylacetylene With n-butyllithium In tetrahydrofuran; hexane at -78℃; Inert atmosphere; Stage #2: (Z)-3-nonenal In tetrahydrofuran; hexane at -78℃; for 2h; Inert atmosphere;	95%

: 31823-43-5
(Z)-3-nonenal

: 3,3-diethoxypropyl triphenylphosphonium iodide

: 118207-20-8
(Z,Z)-dodeca-3,6-dien-1-al diethylacetal

Conditions

Conditions	Yield
Stage #1: 3,3-diethoxypropyl triphenylphosphonium iodide With sodium hexamethyldisilazane In tetrahydrofuran; toluene at 20℃; for 2h; Stage #2: (Z)-3-nonenal In tetrahydrofuran; toluene at -90 - 20℃; Wittig olefination;	88%

: 31823-43-5
(Z)-3-nonenal

: 120379-76-2
[3-[(tert-butyldimethylsilyl)oxy]propyl]triphenylphosphonium bromide

: 125198-05-2
tert-butyl-dodeca-3,6-dienyloxy-dimethylsilane

Conditions

Conditions	Yield
With lithium hexamethyldisilazane In tetrahydrofuran at -78 - 20℃; Condensation;	85%

: C32H34(2)H4O2PS(1+)*Br(1-)

: 31823-43-5
(Z)-3-nonenal

: 947264-17-7
tert-butyl 7-thia(5,6,8,9-2H4)arachidonate

Conditions

Conditions	Yield
Stage #1: C32H34(2)H4O2PS(1+)*Br(1-) With sodium hexamethyldisilazane In tetrahydrofuran; benzene at -78℃; for 0.75h; Stage #2: (Z)-3-nonenal In tetrahydrofuran; benzene at -78 - 20℃; Wittig reaction; Further stages.;	85%

: 31823-43-5
(Z)-3-nonenal

: 420112-17-0
(1E,3E,5Z)-1-bromo-7,7-diethoxyhepta-1,3,5-triene

: (2Z,4E,6E,10Z)-1,1-diethoxyhexadeca-2,4,6,10-tetraen-8-ol

Conditions

Conditions	Yield
Stage #1: (1E,3E,5Z)-1-bromo-7,7-diethoxyhepta-1,3,5-triene With tert.-butyl lithium In diethyl ether; pentane at -75℃; for 1.5h; Stage #2: (Z)-3-nonenal In diethyl ether; pentane at -75℃; for 2h;	76%

: 31823-43-5
(Z)-3-nonenal

: 16666-79-8, 19493-12-0
hexylidenetriphenylphosphoran

: 114832-58-5
cis,cis-6,9-pentadecadiene

Conditions

Conditions	Yield
With sodium hexamethyldisilazane In tetrahydrofuran at -80℃;	75%

: 31823-43-5
(Z)-3-nonenal

: 83606-41-1
((3Z,6Z)-dodeca-3,6-dien-1-yl)triphenylphosphonium bromide

: 54542-68-6
heneicosa-6c,9c,12c,15c-tetraene

Conditions

Conditions	Yield
With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium hexamethyldisilazane In tetrahydrofuran at -78 - 20℃; Condensation;	75%

: 31823-43-5
(Z)-3-nonenal

: (13)C2HLi

: 376591-07-0
C9(13)C2H18O

Conditions

Conditions	Yield
In tetrahydrofuran	71%

: 593-60-2
Vinyl bromide

: 31823-43-5
(Z)-3-nonenal

: 56722-23-7
(5Z)-1,5-undecadien-3-ol

Conditions

Conditions	Yield
With magnesium In tetrahydrofuran 1.) r.t., 6 h; 2.) reflux, 2 h;	70.6%

: 31823-43-5
(Z)-3-nonenal

: 1826-67-1
vinyl magnesium bromide

: 56722-23-7
(5Z)-1,5-undecadien-3-ol

Conditions

Conditions	Yield
In tetrahydrofuran 1. room temp., 8h 2. reflux, 2h;	70%
In diethyl ether at 0℃; for 0.25h; Yield given;
In diethyl ether at 20℃; for 0.5h; Grignard reaction;	2.54 g
In tetrahydrofuran at 0 - 20℃; Grignard Reaction;
In tetrahydrofuran at 0 - 20℃;

: 31823-43-5
(Z)-3-nonenal

: 179681-29-9
(1E,3E,5Z)-1,6-dibromohexa-1,3,5-triene

A: (1E,3E,5Z,9Z)-1-bromo-7-hydroxypentadeca-1,3,5,9-tetraene

B: (1Z,3E,5E,9Z)-1-bromo-7-hydroxy-pentadeca-1,3,5,9-tetraene

C: (6Z,10E,12E,14Z,18Z)-9,16-dihydroxytetraeicosa-6,10,12,14,18-pentaene

Conditions

Conditions	Yield
Stage #1: (1E,3E,5Z)-1,6-dibromohexa-1,3,5-triene With tert.-butyl lithium In diethyl ether; pentane at -75℃; for 1.5h; Stage #2: (Z)-3-nonenal In diethyl ether; pentane at 0℃; for 1.5h;	A 8% B 65% C 10%

...Expand

: 31823-43-5
(Z)-3-nonenal

: 74-86-2
acetylene

: 129030-85-9
(+/-)-(5Z)-5-undecen-1-yn-3-ol

Conditions

Conditions	Yield
With n-butyllithium In tetrahydrofuran at -78℃; for 1h;	62%
With n-butyllithium 1.) THF, hexane, -78 deg C, 20 min, 2.) THF, -78 deg C, 20 min; Yield given. Multistep reaction;
With n-butyllithium 1) THF, hexane, -78 deg C, 30 min., 2) THF, a) -78 deg C, 20 min., b) room temperature, 1 h; Yield given. Multistep reaction;
With n-butyllithium 1.) THF, hexane, -78 deg C, 30 min, 2.a) -78 deg C, 20 min, b) to rt, 1 h; Yield given. Multistep reaction;

: 31823-43-5
(Z)-3-nonenal

: 72036-30-7
ethyl 3-lithiopropiolate

: 76695-83-5
ethyl 4-hydroxy-6-(Z)-dodecen-2-ynoate

Conditions

Conditions	Yield
	60%

: C32H38O2PS(1+)*Br(1-)

: 31823-43-5
(Z)-3-nonenal

: 947264-07-5
tert-butyl 7-thiaarachidonate

Conditions

Conditions	Yield
Stage #1: C32H38O2PS(1+)*Br(1-) With sodium hexamethyldisilazane In tetrahydrofuran; benzene at -78℃; for 0.75h; Stage #2: (Z)-3-nonenal In tetrahydrofuran; benzene at -78 - 20℃; Wittig reaction; Further stages.;	58%

: 31823-43-5
(Z)-3-nonenal

: (1,1-[2H2]-10-methoxycarbonyl-deca-cis,cis-3,6-dienyl)-triphenylphosphonium bromide

: methyl 11-[2H]-arachidonate

Conditions

Conditions	Yield
Stage #1: (1,1-[2H2]-10-methoxycarbonyl-deca-cis,cis-3,6-dienyl)-triphenylphosphonium bromide With sodium hexamethyldisilazane In tetrahydrofuran at -70℃; for 1h; Wittig reaction; Stage #2: (Z)-3-nonenal In tetrahydrofuran at 0℃; for 6h; Wittig reaction; Further stages.;	54%

: 31823-43-5
(Z)-3-nonenal

: 135924-65-1
9-(Triphenyl-λ5-phosphanylidene)-nonanoic acid ethyl ester

: 544-35-4
ethyl (9Z,12Z)-9,12-octadecadienoate

: 31823-43-5
(Z)-3-nonenal

: 58207-97-9
tributyl[(E)-2-trimethylsilylethenyl]stannane

: 115418-86-5
1-(trimethylsilyl)-1(E),5(Z)-undecadien-3(R)-ol

Conditions

Conditions	Yield
With n-butyllithium 1) THF, hexane, -60 deg C, 1h, 2) 0 deg C, 1h; Yield given. Multistep reaction;

: 31823-43-5
(Z)-3-nonenal

: 54655-07-1
lithium trimethylsilylacetylenide

: 118789-62-1
(E/Z)-1-trimethylsilylundec-5-en-1-yn-3-ol

Conditions

Conditions	Yield
In diethyl ether at -30 - 20℃;

: 31823-43-5
(Z)-3-nonenal

: 88730-62-5
Triphenyl-[(Z)-6-(tetrahydro-pyran-2-yloxy)-hex-3-enyl]-phosphonium; iodide

: 120379-60-4
2-((3Z,6Z,9Z)-pentadeca-3,6,9-trienyloxy)tetrahydro-2H-pyran

Conditions

Conditions	Yield
With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium diisopropyl amide 1.) THF, -78 deg C, 1 h, 2.) THF, -78 deg C, 5 min then 0 deg C, 1.5 h; Yield given. Multistep reaction;

: 31823-43-5
(Z)-3-nonenal

: 131721-09-0
Triphenyl-[(1S,4S)-4-(tetrahydro-pyran-2-yloxymethyl)-cyclohex-2-enylmethyl]-phosphonium; iodide

: 131721-10-3
2-[(1S,4R)-((1Z,4Z)-4-Deca-1,4-dienyl)-cyclohex-2-enylmethoxy]-tetrahydro-pyran

Conditions

Conditions	Yield
With n-butyllithium 1.) THF; Multistep reaction;

: 31823-43-5
(Z)-3-nonenal

: 131721-09-0
Triphenyl-[(1S,4R)-4-(tetrahydro-pyran-2-yloxymethyl)-cyclohex-2-enylmethyl]-phosphonium; iodide

: 131721-10-3
2-[(1S,4S)-((1Z,4Z)-4-Deca-1,4-dienyl)-cyclohex-2-enylmethoxy]-tetrahydro-pyran

Conditions

Conditions	Yield
With n-butyllithium 1.) THF; Yield given. Multistep reaction;

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