85329-65-3

Upstream product

• 36049-90-8 2-lithio-1,3-dithiane 
• 85354-57-0 2-[(1R,6R)-6-(3-Iodo-propyl)-2,6-dimethyl-cyclohex-2-enylmethoxy]-tetrahydro-pyran 
• 110-87-2 3,4-dihydro-2H-pyran 
• 85354-55-8 3-((1R,2R)-2-Hydroxymethyl-1,3-dimethyl-cyclohex-3-enyl)-propan-1-ol 
• 85354-56-9 [(1R,6R)-6-(3-Iodo-propyl)-2,6-dimethyl-cyclohex-2-enyl]-methanol 
• 85329-57-3 (1R,2R,4aR,8aR)-2-Ethylamino-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydro-naphthalen-1-ol 
• 85329-53-9 1-((1R,2R,4aR,8aR)-1-Hydroxy-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydro-naphthalen-2-yl)-ethanone 
• 85329-51-7 (R)-2-((1R,2R,4aR,8aR)-1-Hydroxy-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydro-naphthalen-2-yl)-propane-1,2-diol 
• 85329-55-1 N-((1R,2R,4aR,8aR)-1-Hydroxy-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydro-naphthalen-2-yl)-acetamide 
• 68069-04-5 11β-hydroxy-5αH-eudesmanolide 
• 112358-84-6 Toluene-4-sulfonic acid 3-((1R,2R)-2-hydroxymethyl-1,3-dimethyl-cyclohex-3-enyl)-propyl ester 
• 10180-76-4 (3S,3aS,5aR,9aR,9bS)-3,5a,9-Trimethyl-3a,4,5,5a,6,7,9a,9b-octahydro-3H-naphtho[1,2-b]furan-2-one 

Downstream Products

• 85354-58-1 2-((1R,6S)-2,6-Dimethyl-6-{3-[2-(4-methyl-pent-3-enyl)-[1,3]dithian-2-yl]-propyl}-cyclohex-2-enylmethoxy)-tetrahydro-pyran 
• 85440-75-1 [(1R,6S)-2,6-Dimethyl-6-(8-methyl-4-methylene-non-7-enyl)-cyclohex-2-enyl]-methanol 
• 85354-59-2 1-((1S,2R)-2-Hydroxymethyl-1,3-dimethyl-cyclohex-3-enyl)-8-methyl-non-7-en-4-one 

Relevant academic research and scientific papers

Synthesis of 2,6-Dimethyl-6-(8-methyl-4-methylene-7-nonenyl)-2-cyclohexene-1-methanols from α-Santonin

α-Santonin was converted to 2,6-dimethyl-6-(8-methyl-4-methylene-7-nonenyl)-2-cyclohexene-1-methanols (1a and 1b).Both spectral data of 1a and 1b were found to be different from those reported for magydar-2,10(20),13-trien-17-ol, a diterpene isolated from

SYNTHESIS OF 2,6-DIMETHYL-6-(8-METHYL-4-METHYLENE-7-NONENYL)-2-CYCLOHEXEN-1-YLMETHANOLS. A COMMENT ON THE STRUCTURE OF MAGYDAR-2,10(20),13-TRIEN-17-OL, THE DITERPENE OF MAGYDARIS PANACIFOLIA

α-Santonin was stereoselectively converted to a pair of diastereomers of 2,6-dimethyl-6-(8-methyl-4-methylene-7-nonenyl)-2-cyclohexen-1-ylmethanols (Ia and Ib).Both spectral data of Ia and Ib were found to be different from those reported for magydar-2,10