Abstract
Asymmetric osmylation of alkenes by using N,N′-dialkyl-2,2′- bipyrrolidines as the chiral ligands shows a high asymmetric induction and a marked dependence of the enantioselectivity on both the N-alkyl group and the reaction solvent.
| Original language | English |
|---|---|
| Pages (from-to) | 665-666 |
| Number of pages | 2 |
| Journal | Journal of the Chemical Society, Chemical Communications |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - Jan 1 1989 |
| Externally published | Yes |
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All Science Journal Classification (ASJC) codes
- Molecular Medicine
Cite this
Asymmetric dihydroxylation of alkenes with osmium tetroxide : Chiral N,N′-dialkyl-2,2′-bipyrrolidine complex. / Hirama, Masahiro; Oishi, Tohru; Itô, Shô.
In: Journal of the Chemical Society, Chemical Communications, No. 10, 01.01.1989, p. 665-666.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Asymmetric dihydroxylation of alkenes with osmium tetroxide
T2 - Chiral N,N′-dialkyl-2,2′-bipyrrolidine complex
AU - Hirama, Masahiro
AU - Oishi, Tohru
AU - Itô, Shô
PY - 1989/1/1
Y1 - 1989/1/1
N2 - Asymmetric osmylation of alkenes by using N,N′-dialkyl-2,2′- bipyrrolidines as the chiral ligands shows a high asymmetric induction and a marked dependence of the enantioselectivity on both the N-alkyl group and the reaction solvent.
AB - Asymmetric osmylation of alkenes by using N,N′-dialkyl-2,2′- bipyrrolidines as the chiral ligands shows a high asymmetric induction and a marked dependence of the enantioselectivity on both the N-alkyl group and the reaction solvent.
UR - http://www.scopus.com/inward/record.url?scp=37049067929&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=37049067929&partnerID=8YFLogxK
U2 - 10.1039/C39890000665
DO - 10.1039/C39890000665
M3 - Article
AN - SCOPUS:37049067929
SP - 665
EP - 666
JO - Chemical Communications
JF - Chemical Communications
SN - 1359-7345
IS - 10
ER -