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A concise, efficient route to fumitremorgins

✍ Scribed by Patrick D Bailey; Philip J Cochrane; Katrin Lorenz; Ian D Collier; David P.J Pearson; Georgina M Rosair


Book ID
104211443
Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
70 KB
Volume
42
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


Using the kinetically controlled Pictet-Spengler reaction, we have developed a three-step, diastereoselective and enantiospecific synthesis of the natural product demethoxy-fumitremorgin C in 21% overall yield.


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