243117-77-3

Upstream product

• 243117-76-2 dimethyl 2,2,3-trimethyl-3-(2-methoxy-5-methylphenyl)adipate 
• 243117-75-1 2-(5,7-dimethyl-2-oxo-2,3,4,5-tetrahydro-benzo[b]oxepin-5-yl)-2-methyl-propionic acid methyl ester 

Downstream Products

• 81784-10-3 1S-(2'-hydroxy-5'-methylphenyl)-1,2,2-trimethylcyclopentane 
• 220106-58-1 1-methoxy-4-methyl-2-(1,2,2-trimethylcyclopentyl)-benzene 

Relevant academic research and scientific papers

Facile total synthesis of (±)-α-herbertenol, (±)-1,4-cuparenediol and (±)-cuparene-1,4-quinone

The total syntheses of the bicyclic sesquiterpene phenols (±)-α-herbertenol (1) and (±)-1,4-cuparenediol (2) have been successfully accomplished involving copper-catalysed conjugate addition of Grignard reagents to unsaturated dinitriles and α,α-dimethyla

A ring closing metathesis-based approach to (±)-herbertene, (±)-α-herbertenol, (±)-β-herbertenol and (±)-herbertenediol

An efficient methodology for the synthesis of the aromatic sesquiterpenes (±)-herbertene, (±)-α-herbertenol, (±)-β-herbertenol (±)-herbertenediol and (±)-α-cuparenone, employing a combination of Claisen rearrangement and ring closing metathesis reactions,

Facile total synthesis of (±)-α-herbertenol, (±)-α-cuparenone and (±)-HM-1 methyl ether involving alkylation of hindered esters

The total syntheses of (±)-α-herbertenol 1, (±)-α-cuparenone 4 and (±)-HM-1 methyl ether 3 have been successfully accomplished involving α,α- dimethylation of the esters 8a, 17 and 8b respectively as key steps.