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2322-77-2

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Fast Delivery Methoxydienone 2322-77-2 In Stock
Cas No: 2322-77-2
No Data 10 Gram 500 Kilogram/Week WUHAN CIRCLE POWDER TECHNOLOGY CO.,LTD Contact Supplier
Methoxydienone Cutting Cycle Steroids For Sexual Enhancer / Muscle Mass CAS 2322-77-2
Cas No: 2322-77-2
No Data No Data No Data Qingdao little fox Biological &Technology Co.,Ltd Contact Supplier
high purity Trenbolone Enanthate 2322-77-2 Methoxydienone Tren
Cas No: 2322-77-2
USD $ 230.0-250.0 / Gram 10 Gram 50 Kilogram/Day GZ HONESTCHEM CO., LTD Contact Supplier
Methoxydienone Manufacturer/High quality/Best price/In stock
Cas No: 2322-77-2
USD $ 3.0-3.0 / Kilogram 1 Kilogram 1-100 Metric Ton/Month Dayang Chem (Hangzhou) Co.,Ltd. Contact Supplier
Methoxydienone
Cas No: 2322-77-2
No Data 1 Kilogram 30 Metric Ton/Month Simagchem Corporation Contact Supplier
13-beta-ethyl-3-methoxygona-2,5(10)-dien-17-one
Cas No: 2322-77-2
USD $ 40.0-60.0 / Kilogram 1 Kilogram 50 Metric Ton/Year Kono Chem Co.,Ltd Contact Supplier
Methoxydienone Cutting Cycle Steroids For Sexual Enhancer
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USD $ 1.0-3.0 / Kilogram 1 Kilogram 10 Kilogram/Day Hebei yanxi chemical co.,LTD. Contact Supplier
High Quality 99% Gona-2,5(10)-dien-17-one,13-ethyl-3-methoxy- 2322-77-2 ISO Producer
Cas No: 2322-77-2
USD $ 0.1-0.1 / Gram 1 Gram 100 Metric Ton/Year Xi'an Xszo Chem Co., Ltd. Contact Supplier
Factory Supply 13-β-ethyl-3-methoxygona-2,5(10)-dien-17-one
Cas No: 2322-77-2
No Data 1 1 Ality Chemical Corporation Contact Supplier
Methoxydienone Cutting Cycle Steroids For Sexual Enhancer / Muscle Mass
Cas No: 2322-77-2
USD $ 1.0-3.0 / Gram 10 Gram 10000 Kilogram/Month Hebei Yingong New Material Technology Co.,Ltd . Contact Supplier

2322-77-2 Usage

Uses

Max LMG is a progestin derived steroid and not a 17-alpha alkylated steroid. Max LMG is structurally related to RU-486 and acts as an antiprogesterone, decreasing estrogen-like effects.
InChI:InChI=1/C20H28O2/c1-3-20-11-10-16-15-7-5-14(22-2)12-13(15)4-6-17(16)18(20)8-9-19(20)21/h5,16-18H,3-4,6-12H2,1-2H3/t16-,17-,18+,20+/m1/s1

2322-77-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methoxydienone

1.2 Other means of identification

Product number -
Other names 13-Ethyl-3-methoxy-gona-2,5(10)-diene-17-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2322-77-2 SDS

2322-77-2Synthetic route

D-13β-ethyl-17β-hydroxy-3-methoxy-gona-2,5(10)-diene
14507-49-4

D-13β-ethyl-17β-hydroxy-3-methoxy-gona-2,5(10)-diene

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

Conditions
ConditionsYield
With sulfur trioxide pyridine complex In dimethyl sulfoxide; triethylamine Ambient temperature;85%
With molecular sieve; aluminum isopropoxide; butanone In benzene for 12h; Heating;84%
83%
18-methyl-3-methoxy-1,3,5(10),8-estratetraen-17β-ol
7443-72-3

18-methyl-3-methoxy-1,3,5(10),8-estratetraen-17β-ol

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 75 percent / NH3 liq., Li / propan-2-ol; tetrahydrofuran / -45 °C
2: 85 percent / Py*SO3 / dimethylsulfoxide; triethylamine / Ambient temperature
View Scheme
Multi-step reaction with 2 steps
1: (i) LiNH2, liq. NH3, PhNH2, THF, (ii) AcOH, EtOH
2: Al(OiPr)3 / butan-2-one; benzene / Heating
View Scheme
Multi-step reaction with 3 steps
1: ammonium chloride; ammonia / tetrahydrofuran; water; aniline
2: ammonia; lithium / tetrahydrofuran; ethanol; water
View Scheme
Multi-step reaction with 3 steps
1: ammonium chloride; ammonia / tetrahydrofuran; water; aniline
2: ammonia; lithium / tetrahydrofuran; ethanol; water
3: water; cyclohexanone; toluene
View Scheme
2-Trimethylsilyl-1-(4-methoxy-2-methylphenyl)-2-propen-1-on
75863-25-1

2-Trimethylsilyl-1-(4-methoxy-2-methylphenyl)-2-propen-1-on

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 1.) 80 percent NaH; 2.) 10 percent H2SO4 / 1.) DME, parrafin oil, 3.5 h, reflux; Et2O, -20 deg C, 30 min; 2.) MeOH, 24 h
3: 84 percent / mol. sieve, 2-butanone, aluminium isopropylate / benzene / 12 h / Heating
View Scheme
(2R)-2-ethyl-3-vinyl-1-cyclopentanon

(2R)-2-ethyl-3-vinyl-1-cyclopentanon

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 1.) 80 percent NaH; 2.) 10 percent H2SO4 / 1.) DME, parrafin oil, 3.5 h, reflux; Et2O, -20 deg C, 30 min; 2.) MeOH, 24 h
3: 84 percent / mol. sieve, 2-butanone, aluminium isopropylate / benzene / 12 h / Heating
View Scheme
13-Ethyl-3-methoxy-6,7:8,9-disecogona-1,3,5(10),7-tetraen-9,17-dion
101025-85-8

13-Ethyl-3-methoxy-6,7:8,9-disecogona-1,3,5(10),7-tetraen-9,17-dion

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

Conditions
ConditionsYield
Multi-step reaction with 2 steps
2: 84 percent / mol. sieve, 2-butanone, aluminium isopropylate / benzene / 12 h / Heating
View Scheme
13β-Aethyl-3-methoxy-gonapentaen-(1.3.5(10).8.14)-ol-(17β)-acetat
2911-81-1, 5941-86-6, 85760-97-0

13β-Aethyl-3-methoxy-gonapentaen-(1.3.5(10).8.14)-ol-(17β)-acetat

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: H2 / Pd-CaCO3 / benzene; tetrahydrofuran
2: KOH / methanol
3: (i) LiNH2, liq. NH3, PhNH2, THF, (ii) AcOH, EtOH
4: Al(OiPr)3 / butan-2-one; benzene / Heating
View Scheme
13β-ethyl-3-methoxygona-1,3,5(10)8-tetraen-17β-yl acetate
14507-47-2

13β-ethyl-3-methoxygona-1,3,5(10)8-tetraen-17β-yl acetate

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: KOH / methanol
2: (i) LiNH2, liq. NH3, PhNH2, THF, (ii) AcOH, EtOH
3: Al(OiPr)3 / butan-2-one; benzene / Heating
View Scheme
D-13β-ethyl-17β-hydroxy-3-methoxy-gona-2,5(10)-diene
14507-49-4

D-13β-ethyl-17β-hydroxy-3-methoxy-gona-2,5(10)-diene

aluminum isopropoxide
555-31-7

aluminum isopropoxide

sodium sulfate
7757-82-6

sodium sulfate

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

Conditions
ConditionsYield
In water; cyclohexanone; toluene
In water; cyclohexanone; toluene
(+)-17β-hydroxy-13β-ethyl-3-methoxygona-1,3,5(10)-triene
3625-82-9

(+)-17β-hydroxy-13β-ethyl-3-methoxygona-1,3,5(10)-triene

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: ammonia; lithium / tetrahydrofuran; ethanol; water
View Scheme
Multi-step reaction with 2 steps
1: ammonia; lithium / tetrahydrofuran; ethanol; water
2: water; cyclohexanone; toluene
View Scheme
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

DL-13β-ethyl-gon-5(10)-ene-3,17-dione
4222-96-2

DL-13β-ethyl-gon-5(10)-ene-3,17-dione

Conditions
ConditionsYield
With oxalic acid; silica gel In methanol; dichloromethane; water for 0.25h; Ambient temperature;92%
With oxalic acid In dichloromethane; water for 0.333333h; Ambient temperature;87%
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

trimethylsilylacetylene
1066-54-2

trimethylsilylacetylene

levonorgestrel
18316-88-6

levonorgestrel

Conditions
ConditionsYield
Stage #1: trimethylsilylacetylene With n-butyllithium In tetrahydrofuran; hexane at -40 - -20℃; for 1h; Inert atmosphere;
Stage #2: 13β-ethyl-3-methoxygona-2,5(10)-diene-17-one In tetrahydrofuran; hexane at -40℃; for 1h; Inert atmosphere; Further stages;
90%
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

ethylene glycol
107-21-1

ethylene glycol

13β-ethyl-3-methoxy-17,17-ethylenedioxy-gona-2,5(10)-diene
76739-55-4

13β-ethyl-3-methoxy-17,17-ethylenedioxy-gona-2,5(10)-diene

Conditions
ConditionsYield
With toluene-4-sulfonic acid; orthoformic acid triethyl ester at 40℃;80%
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

acetylene
74-86-2

acetylene

13β-ethyl-3-methoxy-17α-ethynyl-gona-2,5(10)-dien-17β-ol
14507-51-8

13β-ethyl-3-methoxy-17α-ethynyl-gona-2,5(10)-dien-17β-ol

Conditions
ConditionsYield
Stage #1: acetylene With potassium tert-butylate In tetrahydrofuran at -10 - 15℃; for 1h; Inert atmosphere;
Stage #2: 13β-ethyl-3-methoxygona-2,5(10)-diene-17-one In tetrahydrofuran at -10 - 0℃; for 3h;
75%
(i) Li, H2NCH2CH2NH2, THF, (ii) aq. H2S; Multistep reaction;
Stage #1: 13β-ethyl-3-methoxygona-2,5(10)-diene-17-one; acetylene With potassium tert-butylate In tetrahydrofuran at -10 - 0℃; for 4h; Inert atmosphere;
Stage #2: With sulfuric acid In tetrahydrofuran; water pH=5 - 6;
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

acetylene
74-86-2

acetylene

levonorgestrel
797-63-7

levonorgestrel

Conditions
ConditionsYield
(i) Li, H2NCH2CH2NH2, THF, (ii) aq. HCl, MeOH; Multistep reaction;
With hydrogenchloride; lithium diisopropyl amide 1.) THF, 2.5 h; 2.) MeOH, 60-70 deg C, 3 h; Yield given. Multistep reaction;
With hydrogenchloride; lithium 1.) ethylenediamine, 1 h; 2.) THF, r.t., 2 h; 3.) MeOH, 45-50 degC, 45 min; Yield given. Multistep reaction;
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

13β-ethyl-17-ethylenedioxo-5(10)-gonen-3-one

13β-ethyl-17-ethylenedioxo-5(10)-gonen-3-one

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 80 percent / HC(OEt)3, p-TsOH / 40 °C
2: 51 percent / oxalic acid, silica gel / CH2Cl2; methanol; H2O / 0.25 h / Ambient temperature
View Scheme
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

DL-13β-ethyl-gona-4,9-diene-3,17-dione
20799-05-7

DL-13β-ethyl-gona-4,9-diene-3,17-dione

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 87 percent / oxalic acid on silica gel / CH2Cl2; H2O / 0.33 h / Ambient temperature
2: 57 percent / pyridinium bromide perbromide / pyridine / Ambient temperature
View Scheme
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

(8S,13S,14S)-13-Ethyl-1,4,6,7,8,12,13,14,15,16-decahydro-2H-cyclopenta[a]phenanthrene-3,17-dione
140221-18-7

(8S,13S,14S)-13-Ethyl-1,4,6,7,8,12,13,14,15,16-decahydro-2H-cyclopenta[a]phenanthrene-3,17-dione

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 87 percent / oxalic acid on silica gel / CH2Cl2; H2O / 0.33 h / Ambient temperature
2: 57 percent / pyridinium bromide perbromide / pyridine / Ambient temperature
3: 95 percent / methanol / 2.5 h / 69 °C
4: 86percent HCOOH / 0.17 h / Ambient temperature
View Scheme
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

DL-13β-ethyl-11β-hydroxy-gon-4-en-3,17-dione

DL-13β-ethyl-11β-hydroxy-gon-4-en-3,17-dione

Conditions
ConditionsYield
Multi-step reaction with 7 steps
1: 87 percent / oxalic acid on silica gel / CH2Cl2; H2O / 0.33 h / Ambient temperature
2: 57 percent / pyridinium bromide perbromide / pyridine / Ambient temperature
3: 95 percent / methanol / 2.5 h / 69 °C
4: 86percent HCOOH / 0.17 h / Ambient temperature
5: O2, Et3N / methanol / 52 h / Ambient temperature
6: 80 percent / NaI, AcOH / methanol / 8 h / Ambient temperature
7: 45 percent / H2, pyridine / 5percent Pd/SrCO3 / 2 h / Ambient temperature
View Scheme
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

DL-13β-ethyl-11β-hydroxy-gona-4,9-dien-3,17-dione
24957-65-1

DL-13β-ethyl-11β-hydroxy-gona-4,9-dien-3,17-dione

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1: 87 percent / oxalic acid on silica gel / CH2Cl2; H2O / 0.33 h / Ambient temperature
2: 57 percent / pyridinium bromide perbromide / pyridine / Ambient temperature
3: 95 percent / methanol / 2.5 h / 69 °C
4: 86percent HCOOH / 0.17 h / Ambient temperature
5: O2, Et3N / methanol / 52 h / Ambient temperature
6: 80 percent / NaI, AcOH / methanol / 8 h / Ambient temperature
View Scheme
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

(8S,11S,13S,14S)-13-Ethyl-11-hydroperoxy-1,6,7,8,11,12,13,14,15,16-decahydro-2H-cyclopenta[a]phenanthrene-3,17-dione
141300-07-4

(8S,11S,13S,14S)-13-Ethyl-11-hydroperoxy-1,6,7,8,11,12,13,14,15,16-decahydro-2H-cyclopenta[a]phenanthrene-3,17-dione

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: 87 percent / oxalic acid on silica gel / CH2Cl2; H2O / 0.33 h / Ambient temperature
2: 57 percent / pyridinium bromide perbromide / pyridine / Ambient temperature
3: 95 percent / methanol / 2.5 h / 69 °C
4: 86percent HCOOH / 0.17 h / Ambient temperature
5: O2, Et3N / methanol / 52 h / Ambient temperature
View Scheme
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

DL-13β-ethyl-3-(N-pyrrolidinyl)-gona-3,5(10),9(11)triene-17-one

DL-13β-ethyl-3-(N-pyrrolidinyl)-gona-3,5(10),9(11)triene-17-one

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 87 percent / oxalic acid on silica gel / CH2Cl2; H2O / 0.33 h / Ambient temperature
2: 57 percent / pyridinium bromide perbromide / pyridine / Ambient temperature
3: 95 percent / methanol / 2.5 h / 69 °C
View Scheme
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

D-17β-acetoxy-13β-ethyl-17α-ethynyl-gon-4-en-3-one
13732-69-9

D-17β-acetoxy-13β-ethyl-17α-ethynyl-gon-4-en-3-one

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: (i) Li, H2NCH2CH2NH2, THF, (ii) aq. HCl, MeOH
2: collidine / Heating
View Scheme
Multi-step reaction with 4 steps
1: tetrahydrofuran; water
2: hydrogenchloride / methanol; water; ethyl acetate; benzene
3: pyridine; acetic anhydride
4: hydrogenchloride; potassium hydroxide; sodium hydrogencarbonate / tetrahydrofuran; methanol
View Scheme
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

dl-13-ethyl-17α-ethynyl-3,17-dihydroxygona-3,5-diene, diacetate
13635-15-9

dl-13-ethyl-17α-ethynyl-3,17-dihydroxygona-3,5-diene, diacetate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: (i) Li, H2NCH2CH2NH2, THF, (ii) aq. HCl, MeOH
2: Py / 160 °C
View Scheme
Multi-step reaction with 3 steps
1: tetrahydrofuran; water
2: hydrogenchloride / methanol; water; ethyl acetate; benzene
3: pyridine; acetic anhydride
View Scheme
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

magnesium sulfate
7487-88-9

magnesium sulfate

13β-ethyl-3-methoxy-17α-ethynyl-gona-2,5(10)-dien-17β-ol
14507-51-8

13β-ethyl-3-methoxy-17α-ethynyl-gona-2,5(10)-dien-17β-ol

Conditions
ConditionsYield
In tetrahydrofuran; water
ethyl bromide
74-96-4

ethyl bromide

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

1-propynylmagnesium bromide
16466-97-0, 13254-27-8

1-propynylmagnesium bromide

13β-ethyl-3-methoxy-17α-propynyl-gona-2,5(10)-dien-17β-ol
854-70-6

13β-ethyl-3-methoxy-17α-propynyl-gona-2,5(10)-dien-17β-ol

Conditions
ConditionsYield
With magnesium In tetrahydrofuran; methanol; water
With magnesium In tetrahydrofuran; methanol; water
1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

lithium chloroacetylide
6180-21-8

lithium chloroacetylide

17α-chloroethynyl-13-ethyl-3-methoxygona-2,5(10)-dien-17β-ol
104577-55-1

17α-chloroethynyl-13-ethyl-3-methoxygona-2,5(10)-dien-17β-ol

Conditions
ConditionsYield
With methyllithium In tetrahydrofuran; (2S)-N-methyl-1-phenylpropan-2-amine hydrate
With methyllithium In tetrahydrofuran; (2S)-N-methyl-1-phenylpropan-2-amine hydrate
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

13β-ethyl-gon-4-en-3,17-dione
21800-83-9

13β-ethyl-gon-4-en-3,17-dione

Conditions
ConditionsYield
With hydrogenchloride; sodium hydrogencarbonate In methanol; water; ethyl acetate
With hydrogenchloride; sodium hydrogencarbonate In methanol; water; ethyl acetate
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

13β-ethyl-3-methoxy-17α-ethynyl-gona-2,5(10)-dien-17β-ol
14507-51-8

13β-ethyl-3-methoxy-17α-ethynyl-gona-2,5(10)-dien-17β-ol

Conditions
ConditionsYield
In tetrahydrofuran; water
13β-ethyl-3-methoxygona-2,5(10)-diene-17-one
2322-77-2

13β-ethyl-3-methoxygona-2,5(10)-diene-17-one

13β-Ethyl-3-methoxy-17α-allyl-gona-2,5(10)-dien-17β-ol
904-92-7

13β-Ethyl-3-methoxy-17α-allyl-gona-2,5(10)-dien-17β-ol

Conditions
ConditionsYield
With magnesium In tetrahydrofuran; methanol; water; allyl bromide
With magnesium In tetrahydrofuran; methanol; water; allyl bromide
With magnesium In tetrahydrofuran; methanol; water; allyl bromide

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