Abstract
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. © 2000 Elsevier Science Ltd.
Original language | English |
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Pages (from-to) | 113-115 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 42 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1 Jan 2001 |
Keywords
- Alkaloids
- Anti-tumour
- Indoles
- Pictet-Spengler