Abstract
The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.
| Original language | English |
|---|---|
| Pages (from-to) | 691-692 |
| Number of pages | 2 |
| Journal | Tetrahedron: Asymmetry |
| Volume | 6 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 1995 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Catalysis
- Inorganic Chemistry
- Organic Chemistry
- Physical and Theoretical Chemistry
- Materials Chemistry
- Drug Discovery
Cite this
Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate : An efficient preparation of a synthetic intermediate of cyclopropane amino acids. / Inoue, Tadashi; Kitagawa, Osamu; Ochiai, Orie; Taguchi, Takeo.
In: Tetrahedron: Asymmetry, Vol. 6, No. 3, 1995, p. 691-692.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate
T2 - An efficient preparation of a synthetic intermediate of cyclopropane amino acids
AU - Inoue, Tadashi
AU - Kitagawa, Osamu
AU - Ochiai, Orie
AU - Taguchi, Takeo
PY - 1995
Y1 - 1995
N2 - The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.
AB - The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.
UR - http://www.scopus.com/inward/record.url?scp=0028918843&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0028918843&partnerID=8YFLogxK
U2 - 10.1016/0957-4166(95)00063-U
DO - 10.1016/0957-4166(95)00063-U
M3 - Article
AN - SCOPUS:0028918843
VL - 6
SP - 691
EP - 692
JO - Tetrahedron Asymmetry
JF - Tetrahedron Asymmetry
SN - 0957-4166
IS - 3
ER -