98719-42-7

Upstream product

• 105735-95-3 (1R,2R,4aS,8aS)-1-(3-Hydroperoxy-3-methyl-pent-4-enyl)-2,5,5,8a-tetramethyl-decahydro-naphthalen-2-ol 
• 78012-27-8 pinnatol A 
• 1093-16-9 8β,20β-Epoxy-manool 
• 1093-16-9 8α,20α-Epoxy-manool 

Downstream Products

• 596-84-9 manoyl oxide 
• 10266-75-8 4-((1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydronaphthalen-1-yl)butan-2-one 
• 596-85-0 (+)-manool 
• 5153-92-4 sclareol oxide 
• 14506-65-1 15,16-dinor-labd-8-en-13-one 
• 39707-56-7 (+)-zonarone 
• 39707-59-0 ent-isozonarone 
• 39707-54-5 (-)-ent-zonarol 
• 250146-75-9 ent-isozonarol 
• 1376654-34-0 (+)-yahazunone 
• 597541-58-7 Toluene-4-sulfonic acid (2S,3S)-3-methyl-3-[2-(3,4,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-ethyl]-oxiranylmethyl ester 
• 6790-58-5 (-)-ambroxide 

Relevant academic research and scientific papers

STRUCTURE OF NEW BROMODITERPENES, PINNATOLS, FROM THE MARINE RED ALGA LAURENCIA PINNATA YAMADA

The structure of new bromoditerpenes named pinnatols A, B, C, and D, isolated from the title alga, was determined on the basis of the chemical and spectral data.

A SHORT SYNTHESIS OF AMBROX FROM SCLAREOL

A two-step transformation of sclareol into Ambrox (overall yield 11-12percent) via β-cleavage of an alkoxy radical intermediate is described.