50657-30-2

Upstream product

• 139686-92-3 (1R,2S,5R,7R)-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undecan-8-one 
• 139640-16-7 (3S,3aR,6R,7aR,9S)-9-Benzyloxy-3,6,7,7-tetramethyl-octahydro-3a,6-ethano-indene 
• 139640-15-6 (1S,5R,7R,8S)-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undec-2-en-8-ol 
• 139640-18-9 (1S,2R,3R,5R,7R, 8S)-8-benzyloxy-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undecan-3-ol 
• 139640-17-8 (1S,5R,5R,8S)-8-benzyloxy-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undec-2-ene 
• 139640-20-3 (1S,2R,5R,7R,8S)-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undecan-3-one 
• 139640-19-0 (1S,2R,3R,5R,7R,8S)-8-benzyloxy-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undec-3-yl methanesulfonate 
• 139640-15-6 (1S,5R,7R,8R)-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undec-2-en-8-ol 
• 139686-92-3 khusione 
• 1372617-30-5 C₁₅H₂₆O₂ 
• 1372617-32-7 C₂₂H₂₈O₃ 
• 1372617-31-6 C₁₅H₂₄O₂ 
• 1372617-29-2 C₁₈H₃₀O₂ 
• 50657-30-2 khusian-2-ol 

Downstream Products

• 139686-90-1 (1R,2S,5R,7R,8S)-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undecan-8-ol 
• 50657-30-2 Epikhusiol 

Relevant academic research and scientific papers

Approaches to the neurotrophically active natural product 11-O-debenzoyltashironin: A chemoenzymatic total synthesis of the structurally related sesquiterpene khusiol

Soothes your nerves: The enantiomerically enriched cis-1,2-dihydrocatechol 4 has been converted, over 16 steps including one involving an intramolecular Diels-Alder reaction, into the sesquiterpenoid natural product khusiol (3), which is structurally related to the neurite outgrowth-promoting natural product 11-O-debenzoyltashironin (1).

The Biogenetic-Type Cyclization of the Unsaturated Monocyclic Alcohol with Formic Acid; Factile Synthesis of the Tricarbocyclic Alcohol, (+)-2-Epi-allo-cedrol

The biogenetic-type cyclization of (+)-(3S)-2-(3-hydroxy-3-methyl-4-pentenyl)-1-methyl-3-(1-methylethenyl)-cyclopentene, prepared from d-limonene, with formic acid gave stereo and regiospecifically the formates of the tricyclic compounds of the allo-cedro