Abstract
The thermal cyclization of γ-aminoallylstannane (8) having an aldehyde group gave β-hydroxypyrrolidine derivative (9a) as a sole product. This methodology was applied successfully to the total synthesis of (+)-preussin.
| Original language | English |
|---|---|
| Pages (from-to) | 335-348 |
| Number of pages | 14 |
| Journal | Heterocycles |
| Volume | 46 |
| Issue number | 1 |
| Publication status | Published - 1997 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Organic Chemistry
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Novel route to the synthesis of hydroxylated pyrrolidine derivatives via the intramolecular reaction of γ-aminoallylstannane with aldehyde. Total synthesis of (+)-preussin. / Kadota, Isao; Saya, Shioko; Yamamoto, Yoshinori.
In: Heterocycles, Vol. 46, No. 1, 1997, p. 335-348.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Novel route to the synthesis of hydroxylated pyrrolidine derivatives via the intramolecular reaction of γ-aminoallylstannane with aldehyde. Total synthesis of (+)-preussin
AU - Kadota, Isao
AU - Saya, Shioko
AU - Yamamoto, Yoshinori
PY - 1997
Y1 - 1997
N2 - The thermal cyclization of γ-aminoallylstannane (8) having an aldehyde group gave β-hydroxypyrrolidine derivative (9a) as a sole product. This methodology was applied successfully to the total synthesis of (+)-preussin.
AB - The thermal cyclization of γ-aminoallylstannane (8) having an aldehyde group gave β-hydroxypyrrolidine derivative (9a) as a sole product. This methodology was applied successfully to the total synthesis of (+)-preussin.
UR - http://www.scopus.com/inward/record.url?scp=0000391968&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0000391968&partnerID=8YFLogxK
M3 - Article
VL - 46
SP - 335
EP - 348
JO - Heterocycles
JF - Heterocycles
SN - 0385-5414
IS - 1
ER -