Abstract
Enolate dianion of diethyl (S)-malate was stereoselectively condensed with nonenoiizable N-arylimines to give 2-pyrrolidinone derivatives. The presence of HMPA changes the diastereoselectivity of this cyclization reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 8445-8448 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 36 |
| Issue number | 46 |
| DOIs | |
| Publication status | Published - 1995 Nov 13 |
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ASJC Scopus subject areas
- Drug Discovery
- Organic Chemistry
- Biochemistry
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Stereoselectivity in the condensation reactions between malate enolate and imines to 2-pyrrolidinone derivatives. / Ha, Deok-Chan; Yun, Kyeong Soon; Park, Hye Sang; Choung, Won Keun; Kwon, Young Eun.
In: Tetrahedron Letters, Vol. 36, No. 46, 13.11.1995, p. 8445-8448.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Stereoselectivity in the condensation reactions between malate enolate and imines to 2-pyrrolidinone derivatives
AU - Ha, Deok-Chan
AU - Yun, Kyeong Soon
AU - Park, Hye Sang
AU - Choung, Won Keun
AU - Kwon, Young Eun
PY - 1995/11/13
Y1 - 1995/11/13
N2 - Enolate dianion of diethyl (S)-malate was stereoselectively condensed with nonenoiizable N-arylimines to give 2-pyrrolidinone derivatives. The presence of HMPA changes the diastereoselectivity of this cyclization reaction.
AB - Enolate dianion of diethyl (S)-malate was stereoselectively condensed with nonenoiizable N-arylimines to give 2-pyrrolidinone derivatives. The presence of HMPA changes the diastereoselectivity of this cyclization reaction.
UR - http://www.scopus.com/inward/record.url?scp=0028837696&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0028837696&partnerID=8YFLogxK
U2 - 10.1016/0040-4039(95)01818-3
DO - 10.1016/0040-4039(95)01818-3
M3 - Article
AN - SCOPUS:0028837696
VL - 36
SP - 8445
EP - 8448
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 46
ER -