164229-08-7

Upstream product

• 187462-84-6 (1S,4R,5R)-4-Benzyloxymethyl-2-oxa-bicyclo[3.2.1]octan-3-ol 
• 17482-09-6 benzyl iodomethyl ether 
• 187462-85-7 (R)-3-((R)-1-Benzyloxymethyl-allyl)-cyclopentanol 

Downstream Products

• 164229-09-8 (S)-3-((R)-1-Benzyloxymethyl-allyl)-6,10-dithia-spiro[4.5]decan-1-one 
• 187462-92-6 [(R)-2-((S)-4-Oxo-6,10-dithia-spiro[4.5]dec-2-yl)-but-3-enyl]-carbamic acid benzyl ester 
• 187462-94-8 C₂₀H₂₃NO₃S₂ 
• 187462-93-7 [(R)-2-((S)-3-Iodo-4-oxo-6,10-dithia-spiro[4.5]dec-2-yl)-but-3-enyl]-carbamic acid benzyl ester 

Relevant academic research and scientific papers

A new enantiocontrolled route to (-)-kainic acid

A new route to (-)-kainic acid, the parent member of the kainoids, has been developed using (+)-norcamphor as the starting material.

Enantio- and stereocontrolled synthesis of (-)-semburin, (+)-N-benzoylmeroquinene aldehyde, (-)-antirhine, and (+)-isocorynantheol from common (+)-norcamphor

A general enantio- and stereocontrolled route to the representative secologanin natural products, (-)-semburin, (+)-N-benzoylmeroquinene aldehyde, (-)-antirhine, and (+)-isocorynantheol, has been developed starting from (+)-norcamphor as a common chiral b