Abstract
Slaframine (1) has been synthesized from diene aldehyde 2. An intramolecular imino Diels-Alder reaction has been used to produce the indolizidine skeleton and to establish the requisite stereochemistry of this fungal metabolite.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 7065-7068 |
| Number of pages | 4 |
| Journal | Journal of the American Chemical Society |
| Volume | 104 |
| Issue number | 25 |
| DOIs | |
| State | Published - Jan 1 1982 |
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All Science Journal Classification (ASJC) codes
- Catalysis
- Chemistry(all)
- Biochemistry
- Colloid and Surface Chemistry
Cite this
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A New Total Synthesis of the Fungal Toxin Slaframine. / Gobao, Richard A.; Bremmer, Martin L.; Weinreb, Steven M.
In: Journal of the American Chemical Society, Vol. 104, No. 25, 01.01.1982, p. 7065-7068.Research output: Contribution to journal › Article
TY - JOUR
T1 - A New Total Synthesis of the Fungal Toxin Slaframine
AU - Gobao, Richard A.
AU - Bremmer, Martin L.
AU - Weinreb, Steven M.
PY - 1982/1/1
Y1 - 1982/1/1
N2 - Slaframine (1) has been synthesized from diene aldehyde 2. An intramolecular imino Diels-Alder reaction has been used to produce the indolizidine skeleton and to establish the requisite stereochemistry of this fungal metabolite.
AB - Slaframine (1) has been synthesized from diene aldehyde 2. An intramolecular imino Diels-Alder reaction has been used to produce the indolizidine skeleton and to establish the requisite stereochemistry of this fungal metabolite.
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UR - http://www.scopus.com/inward/citedby.url?scp=0020445799&partnerID=8YFLogxK
U2 - 10.1021/ja00389a030
DO - 10.1021/ja00389a030
M3 - Article
VL - 104
SP - 7065
EP - 7068
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 25
ER -