CAS No.5090-54-0,VALERANONE Suppliers

Shanghai Upbio Tech Co.,Ltd

1.In No Less 10 years exporting experience. you can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specializ

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Shandong Hanjiang Chemical Co., Ltd.

Hello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai

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Henan Wentao Chemical Product Co., Ltd.

Henan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod

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TAIZHOU ZHENYU BIOTECHNOLOGY CO., LTD

Zhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed

VALERANONE

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KAISA GROUP INC

1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer

5090-54-0 CAS NO.5090-54-0

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Henan Tianfu Chemical Co., Ltd.

1.Our services：A.Supply sampleB.The packing also can be according the customers` requirmentC.Any inquiries will be replied within 24 hoursD.we provide Commerical Invoice, Packing List, Bill of loading, COA , Health certificate and Origin certificate.

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BOC Sciences

We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:white to yellow crystal powder Storage:Room temperature with sealed well Package:according to the clients requirement Applicatio

(7R)-4a,8a-dimethyl-7-propan-2-yl-3,4,5,6,7,8-hexahydro-2H-naphthalen-1-one

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Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

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Changchun Artel lmport and Export trade company

Supply top quality products with a reasonable price Application:api

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Henan Kanbei Chemical Co.,LTD

factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin

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Shanghai Chinqesen Biotechnology Co., Ltd.

Good Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen

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Chemlyte Solutions

Stock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai

(7R)-4a,8a-dimethyl-7-propan-2-yl-3,4,5,6,7,8-hexahydro-2H-naphthalen-1-one

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Shanghai Terui OP New Material Technology Co., Ltd.

The factory supplies Application:manufacturing supplies

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ZHEJIANG JIUZHOU CHEM CO.,LTD

factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin

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Changzhou Extraordinary Pharmatech co.,LTD

Changzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa

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Jilin haofei import and export trade Co.,Ltd

Price, service, company and transport advantage: 1. Best service, place of origin China, high quality, and reasonable price. 2. It's customers' right to choose the package (EMS, DHL, FEDEX, UPS). 3. It's customers' right

5090-54-0 CAS NO.5090-54-0

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Nanjing Raymon Biotech Co., Ltd.

( )-ValeranoneAppearance:Off white to slight yellow solid Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By courier like DH

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Chemical Co.Ltd

( )-ValeranoneAppearance: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 su

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Alfa Chemistry

(?)-Valeranone

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Synthetic route

: 177533-01-6
(1R,6R,9R)-1,6-dimethyl-9-isopropylbicyclo[4.4.0]dec-3-en-2-one

: 5090-54-0
valeranone

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In methanol for 12h;	80%
With hydrogen; palladium on activated charcoal In methanol under 760 Torr; for 12h;	80%

: 2212-97-7, 106707-55-5
Deoxyfauronol-aethylenketal

: 5090-54-0
valeranone

Conditions

Conditions	Yield
With hydrogenchloride

: 4893-79-2, 98573-74-1
8,8-Aethylendioxy-(2R)-isopropyl-(4aR)-hydroxymethyl-(8aR)-methyl-dekalin

: 5090-54-0
valeranone

Conditions

Conditions	Yield
(i) CrO3, Py, (ii) N2H4*H2O, KOH, (iii) aq. AcOH; Multistep reaction;

: 16735-11-8, 66510-89-2
(1aR,4aS,7R,8aS)-7-Isopropyl-1a-methoxy-4a-methyl-decahydro-cyclopropa[d]naphthalene

: 5090-54-0
valeranone

Conditions

Conditions	Yield
With hydrogenchloride

: 823203-43-6
(1S,3aR,6R,7aS)-2-Iodo-6-isopropyl-1,3a,7a-trimethyl-octahydro-indene

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dimethylformamide / 0.5 h / 160 °C 1.2: ozone / methanol; CH2Cl2 / -78 °C 1.3: triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C 2.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 3.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

: 823203-42-5
(1S,3R,6R,9S)-3-isopropyl-1,6,9-trimethylbicyclo[4.3.0]nonan-8-ol

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1.1: 76 percent / iodine; triphenylphosphine; imidazole / benzene / 2 h / 20 °C 2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dimethylformamide / 0.5 h / 160 °C 2.2: ozone / methanol; CH2Cl2 / -78 °C 2.3: triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C 3.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 4.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

Yield

Multi-step reaction with 4 steps
1.1: 76 percent / iodine; triphenylphosphine; imidazole / benzene / 2 h / 20 °C
2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dimethylformamide / 0.5 h / 160 °C
2.2: ozone / methanol; CH2Cl2 / -78 °C
2.3: triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C
3.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C
4.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr
View Scheme

: 177532-97-7
(1R,2R,4R)-1,2,-dimethyl-2-(1-hydroxyethyl)-4-isopropylcyclohexaneethanol

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 6 steps 1: 65 percent / imidazole / CH2Cl2 / 1 h / 0 °C 2: 82 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 3: 70 percent / tetrabutylammonium fluoride / tetrahydrofuran / 4 h / 20 °C 4: 72 percent / PCC; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 5: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 6: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

Yield

Multi-step reaction with 6 steps
1: 65 percent / imidazole / CH2Cl2 / 1 h / 0 °C
2: 82 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 0.5 h / 20 °C
3: 70 percent / tetrabutylammonium fluoride / tetrahydrofuran / 4 h / 20 °C
4: 72 percent / PCC; sodium acetate / CH2Cl2 / 0.5 h / 20 °C
5: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C
6: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr
View Scheme

: 177532-94-4
(1S,3R,6R,9S)-3-isopropenyl-1,6,9-trimethylbicyclo[4.3.0]nonan-8-one

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 6 steps 1.1: 99 percent / H2 / Pd/C / methanol / 12 h 2.1: 96 percent / NaBH4 / methanol / 0.25 h / cooling 3.1: 76 percent / iodine; triphenylphosphine; imidazole / benzene / 2 h / 20 °C 4.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dimethylformamide / 0.5 h / 160 °C 4.2: ozone / methanol; CH2Cl2 / -78 °C 4.3: triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C 5.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 6.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme
Multi-step reaction with 4 steps 1: 98 percent / H2 / 10percent Pd/C / methanol / 6 h 2: 1.) NaBH4, 2.) PPh3, iodine, imidazole / 1.) MeOH, 0 deg C, 15 min, 2.) C6H6, room temperature 2 h 4: 80 percent / H2 / 10percent Pd/C / methanol / 12 h View Scheme

Yield

Multi-step reaction with 6 steps
1.1: 99 percent / H2 / Pd/C / methanol / 12 h
2.1: 96 percent / NaBH4 / methanol / 0.25 h / cooling
3.1: 76 percent / iodine; triphenylphosphine; imidazole / benzene / 2 h / 20 °C
4.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dimethylformamide / 0.5 h / 160 °C
4.2: ozone / methanol; CH2Cl2 / -78 °C
4.3: triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C
5.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C
6.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr
View Scheme

Multi-step reaction with 4 steps
1: 98 percent / H2 / 10percent Pd/C / methanol / 6 h
2: 1.) NaBH4, 2.) PPh3, iodine, imidazole / 1.) MeOH, 0 deg C, 15 min, 2.) C6H6, room temperature 2 h
4: 80 percent / H2 / 10percent Pd/C / methanol / 12 h
View Scheme

: 177532-95-5
(1S,3R,6R,9S)-3-isopropyl-1,6,9-trimethylbicyclo[4.3.0]nonan-8-one

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1.1: 96 percent / NaBH4 / methanol / 0.25 h / cooling 2.1: 76 percent / iodine; triphenylphosphine; imidazole / benzene / 2 h / 20 °C 3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dimethylformamide / 0.5 h / 160 °C 3.2: ozone / methanol; CH2Cl2 / -78 °C 3.3: triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C 4.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 5.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme
Multi-step reaction with 3 steps 1: 1.) NaBH4, 2.) PPh3, iodine, imidazole / 1.) MeOH, 0 deg C, 15 min, 2.) C6H6, room temperature 2 h 3: 80 percent / H2 / 10percent Pd/C / methanol / 12 h View Scheme

Yield

Multi-step reaction with 5 steps
1.1: 96 percent / NaBH4 / methanol / 0.25 h / cooling
2.1: 76 percent / iodine; triphenylphosphine; imidazole / benzene / 2 h / 20 °C
3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dimethylformamide / 0.5 h / 160 °C
3.2: ozone / methanol; CH2Cl2 / -78 °C
3.3: triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C
4.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C
5.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr
View Scheme

Multi-step reaction with 3 steps
1: 1.) NaBH4, 2.) PPh3, iodine, imidazole / 1.) MeOH, 0 deg C, 15 min, 2.) C6H6, room temperature 2 h
3: 80 percent / H2 / 10percent Pd/C / methanol / 12 h
View Scheme

: 177532-96-6
(1R,2S,6R,9R)-9-isopropyl-1,2,6-trimethyl-3-oxabicyclo[4.4.0]decan-4-one

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 7 steps 1: 98 percent / lithium aluminium hydride / diethyl ether / 0.5 h / 20 °C 2: 65 percent / imidazole / CH2Cl2 / 1 h / 0 °C 3: 82 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 4: 70 percent / tetrabutylammonium fluoride / tetrahydrofuran / 4 h / 20 °C 5: 72 percent / PCC; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 6: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 7: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme
Multi-step reaction with 6 steps 1.1: 87 percent / diisobutylaluminium hydride / toluene / 1 h / -78 °C 2.1: 57 percent / tetrahydrofuran / 1 h / 40 °C 3.1: 80 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 4.1: ozone / methanol; CH2Cl2 / -75 °C 4.2: 75 percent / triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C 5.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 6.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

Yield

Multi-step reaction with 7 steps
1: 98 percent / lithium aluminium hydride / diethyl ether / 0.5 h / 20 °C
2: 65 percent / imidazole / CH2Cl2 / 1 h / 0 °C
3: 82 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 0.5 h / 20 °C
4: 70 percent / tetrabutylammonium fluoride / tetrahydrofuran / 4 h / 20 °C
5: 72 percent / PCC; sodium acetate / CH2Cl2 / 0.5 h / 20 °C
6: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C
7: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr
View Scheme

Multi-step reaction with 6 steps
1.1: 87 percent / diisobutylaluminium hydride / toluene / 1 h / -78 °C
2.1: 57 percent / tetrahydrofuran / 1 h / 40 °C
3.1: 80 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 0.5 h / 20 °C
4.1: ozone / methanol; CH2Cl2 / -75 °C
4.2: 75 percent / triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C
5.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C
6.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr
View Scheme

: 261957-25-9
2-[(1R,2R,4R)-2-acetyl-4-isopropyl-1,2-dimethylcyclohexyl]acetaldehyde

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 2: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

: 261957-31-7
1-[(1R,2R,5R)-(2-allyl-5-isopropyl-1,2-dimethylcyclohexyl)]ethanone

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: ozone / methanol; CH2Cl2 / -75 °C 1.2: 75 percent / triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C 2.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 3.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

: 261957-30-6
(1S)-1-[(1R,2R,5R)-(2-allyl-5-isopropyl-1,2-dimethylcyclohexyl)]ethanol

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1.1: 80 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 2.1: ozone / methanol; CH2Cl2 / -75 °C 2.2: 75 percent / triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C 3.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 4.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

: 261957-28-2
(1R,6R,9R)-9-isopropyl-1,2,6-trimethyl-3-oxabicyclo[4.4.0]decan-2-ol

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 72 percent / PCC; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 2: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 3: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

: 261957-29-3
(1R,2R,6R,9R)-9-isopropyl-1,2,6-trimethyl-3-oxabicyclo[4.4.0]decan-4-ol

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1.1: 57 percent / tetrahydrofuran / 1 h / 40 °C 2.1: 80 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 3.1: ozone / methanol; CH2Cl2 / -75 °C 3.2: 75 percent / triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C 4.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 5.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

Yield

Multi-step reaction with 5 steps
1.1: 57 percent / tetrahydrofuran / 1 h / 40 °C
2.1: 80 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 0.5 h / 20 °C
3.1: ozone / methanol; CH2Cl2 / -75 °C
3.2: 75 percent / triphenylphosphine / methanol; CH2Cl2 / 8 h / 20 °C
4.1: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C
5.1: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr
View Scheme

: 261957-27-1
1-[(1R,2R,5R)-2-(2-tert-butyldimethylsilyloxyethyl)-5-isopropyl-1,2-dimethylcyclohexyl]-1-ethanone

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 70 percent / tetrabutylammonium fluoride / tetrahydrofuran / 4 h / 20 °C 2: 72 percent / PCC; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 3: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 4: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

: 261957-26-0
(1S)-1-[(1R,2R,5R)-2-(tert-butyldimethylsilyloxyethyl)-5-isopropyl-1,2-dimethylcyclohexyl]ethanol

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: 82 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 2: 70 percent / tetrabutylammonium fluoride / tetrahydrofuran / 4 h / 20 °C 3: 72 percent / PCC; sodium acetate / CH2Cl2 / 0.5 h / 20 °C 4: 76 percent / KOH / tetrahydrofuran; methanol; H2O / 8 h / 20 °C 5: 80 percent / H2 / Pd/C / methanol / 12 h / 760 Torr View Scheme

: (3aR,6R,7aS)-2-Iodo-6-isopropyl-1,3a,7a-trimethyl-octahydro-indene

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 2: 80 percent / H2 / 10percent Pd/C / methanol / 12 h View Scheme

: 16840-48-5
5ξ-Hydroxy-7β-isopropyl-4ξ-methoxy-10α-methyl-3-decalon

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 6 steps 1: KOH 2: LiAlH4 3: I2, Zn-Cu 4: CrO3, H2SO4 5: N2H4, diethylene glycol, KOH 6: aq. HCl View Scheme

: 16735-09-4, 66510-87-0
7β-Isopropyl-4β-methoxy-10α-methyl-4α,5α-methylen-3α-decalol

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: CrO3, H2SO4 2: N2H4, diethylene glycol, KOH 3: aq. HCl View Scheme

: 66510-86-9
7β-Isopropyl-4-methoxy-10α-methyl-4-octalin-3α-ol

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: I2, Zn-Cu 2: CrO3, H2SO4 3: N2H4, diethylene glycol, KOH 4: aq. HCl View Scheme

: 16735-10-7, 66510-88-1
(1aR,4aR,7R,8aS)-7-Isopropyl-1a-methoxy-4a-methyl-octahydro-cyclopropa[d]naphthalen-2-one

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: N2H4, diethylene glycol, KOH 2: aq. HCl View Scheme

: 66334-13-2
7β-Isopropyl-4-methoxy-10α-methyl-4-octalin-3-on

: 5090-54-0
valeranone

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: LiAlH4 2: I2, Zn-Cu 3: CrO3, H2SO4 4: N2H4, diethylene glycol, KOH 5: aq. HCl View Scheme

: 5090-54-0
valeranone

: 4893-70-3, 4893-71-4, 17408-73-0, 114127-46-7, 114127-47-8
(4aS)-7t-Isopropyl-4a,8a-dimethyl-(4ar,8ac)-decahydro-[1c]naphthol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride; diethyl ether
With lithium aluminium tetrahydride

: 5090-54-0
valeranone

: 2658-90-4, 18866-65-4
(4aR)-2ξ-bromo-7t-isopropyl-4a,8a-dimethyl-(4ar,8ac)-octahydro-naphthalen-1-one

Conditions

Conditions	Yield
With bromine
With bromine In acetic acid

: 186581-53-3, 908094-01-9
diazomethane

: 5090-54-0
valeranone

: Trisnorphotovaleronsaeuremethylester

Conditions

Conditions	Yield
Multistep reaction;

: 186581-53-3, 908094-01-9
diazomethane

: 5090-54-0
valeranone

: Bisnorphotovaleronsaeuremethylester

Conditions

Conditions	Yield
Multistep reaction;

: 186581-53-3, 908094-01-9
diazomethane

: 5090-54-0
valeranone

: Norphotovaleronsaeuremethylester

Conditions

Conditions	Yield
Multistep reaction;

: 186581-53-3, 908094-01-9
diazomethane

: 5090-54-0
valeranone

: Photovaleronsaeuremethylester

Conditions

Conditions	Yield
(i) (UV-irradiation), (ii) /BRN= 102415/; Multistep reaction;

: 5090-54-0
valeranone

: 5050-72-6
(1R,3R,6S)-3-Isopropyl-1,6-dimethylbicyclo[4.4.0]decane

Conditions

Conditions	Yield
With potassium hydroxide; hydrazine at 180 - 190℃;
With sodium; hydrazine hydrate
Multi-step reaction with 2 steps 1: (i) LiAlH4, (ii) phthalic anhydride 2: H2 / PtO2 View Scheme

: 5090-54-0
valeranone

A: 4893-70-3, 4893-71-4, 17408-73-0, 114127-46-7, 114127-47-8
(4aS)-7t-Isopropyl-4a,8a-dimethyl-(4ar,8ac)-decahydro-[1c]naphthol

B: 4893-70-3, 4893-71-4, 17408-73-0, 114127-46-7, 114127-47-8
4-epi-Valeranol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In diethyl ether Heating;

: 5090-54-0
valeranone

: 4893-70-3, 4893-71-4, 17408-73-0, 114127-46-7, 114127-47-8
4-epi-Valeranol

Conditions

Conditions	Yield
With sodium ethanolate In ethanol

: 5090-54-0
valeranone

: (4aR)-2,2-dibromo-7t-isopropyl-4a,8a-dimethyl-(4ar,8ac)-octahydro-naphthalen-1-one

Conditions

Conditions	Yield
With bromine In acetic acid

: 5090-54-0
valeranone

: 177186-97-9
Jatamansen

Conditions

Conditions	Yield
(i) LiAlH4, (ii) phthalic anhydride; Multistep reaction;

: 5090-54-0
valeranone

: Trisnorphotovaleronsaeure

Conditions

Conditions	Yield
Multistep reaction;

: 5090-54-0
valeranone

: Bisnorphotovaleronsaeure

Conditions

Conditions	Yield
Multistep reaction;

: 5090-54-0
valeranone

: Norphotovaleronsaeure

Conditions

Conditions	Yield
Multistep reaction;

: 5090-54-0
valeranone

: Photovaleronsaeure

Conditions

Conditions	Yield
In acetic acid Irradiation;

: 5090-54-0
valeranone

: 100-52-7
benzaldehyde

: 100270-35-7
(4aR)-2-((Ξ)-benzylidene)-7t-isopropyl-4a,8a-dimethyl-(4ar,8ac)-octahydro-naphthalen-1-one

Conditions

Conditions	Yield
With sodium ethanolate
(i) HCl, (ii) NaOAc; Multistep reaction;

: 186581-53-3, 908094-01-9
diazomethane

: 5090-54-0
valeranone

: 5487-10-5, 93190-80-8
Hydroxyvaleranosaeuremethylester

Conditions

Conditions	Yield
(i) PhCO3H, (ii) (hydrolysis), (iii) /BRN= 102415/; Multistep reaction;

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