699010-02-1

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 699010-01-0 (1S)-1-{(2S,5R)-5-[(1R)-1-hydroxytridecyl]tetrahydrofuran-2-yl}ethane-1,2-diol 
• 145285-55-8 trans ethyl heptadec-4-enoate 
• 184435-63-0 (4E)-heptadec-4-enal 
• 699009-91-1 (2S)-N-[(R)-2-hydroxy-2-[(2S,5R)-5-((R)-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 

Relevant academic research and scientific papers

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

Total synthesis and stereochemical assignment of cis-uvariamicin I and cis-reticulatacin

(Graph Presented) Diastereoisomeric mixtures of cis-uvariamicin I (15R,16R,19S,20S,36S and 15S,16S,19R,20R,36S) and cis-reticulatacin (17R,18R,21S,22S,36S and 17S,18S,21R,22R,36S) were synthesized to determine the stereochemistry of the natural products i