699009-95-5

Upstream product

• 476310-00-6 (2S)-N-[(S)-2-hydroxy-2-[(2R,5S)-5-((S)-1-hydroxytridecyl)tetrahydro-2-furanyl]ethanoyl]camphor-10,2-sultam 
• 476310-01-7 (2S)-N-((2E,6E)-2,6-nonadecadienoyl)camphor-10,2-sultam 
• 849337-21-9 (2E,6E)-nonadeca-2,6-dienoyl chloride 
• 699009-90-0 (2E,6E)-nonadeca-2,6-dienoic acid 
• 184435-64-1 ethyl (2E,6E)-nonadeca-2,6-dienoate 
• 184435-63-0 (4E)-heptadec-4-enal 
• 145285-55-8 trans ethyl heptadec-4-enoate 
• 98-59-9 p-toluenesulfonyl chloride 
• 699009-94-4 (1R)-1-{(2R,5S)-5-[(1S)-1-hydroxytridecyl]tetrahydrofuran-2-yl}ethane-1,2-diol 

Relevant academic research and scientific papers

Oxidative cyclization of diols derived from 1,5-dienes: Formation of enantiopure cis-tetrahydrofurans by using catalytic osmium tetroxide; formal synthesis of (+)-cis-solamin

(Chemical Equation Presented) High yields and high levels of stereocontrol are observed in the oxidative cyclization of vicinal diols using catalytic amounts of a transition metal (see scheme; TFA = trifluoroacetic acid). The product stereochemistry is co

Total Synthesis and Preliminary Biological Evaluation of cis-Solamin Isomers

An efficient total synthesis of cis-solamin (1) has been achieved in 21% overall yield and with a longest linear sequence of just 11 steps from aldehyde 8. A key feature of the approach was the use of asymmetric permanganate-promoted oxidative cyclization