139640-16-7

Upstream product

• 100-39-0 benzyl bromide 
• 139640-14-5 Formic acid (3aR,6S,7aR)-3,6,7,7-tetramethyl-1,4,5,6,7,7a-hexahydro-3a,6-ethano-inden-9-yl ester 
• 139640-15-6 (1S,5R,7R,8S)-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undec-2-en-8-ol 
• 139640-17-8 (1S,5R,5R,8S)-8-benzyloxy-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undec-2-ene 
• 139640-18-9 (1S,2R,3R,5R,7R, 8S)-8-benzyloxy-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undecan-3-ol 
• 139640-19-0 (1S,2R,3R,5R,7R,8S)-8-benzyloxy-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undec-3-yl methanesulfonate 
• 139640-20-3 (1S,2R,5R,7R,8S)-2,6,6,7-tetramethyltricyclo<5.2.2.0^1,5>undecan-3-one 

Downstream Products

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

Relevant academic research and scientific papers

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