Abstract
Nucleophilic addition to substituted γ- and δ-lactols with titanium reagents provides 1,4-syn and 1,5-syn diols in high stereoselectivity, which represents a new and simple method for the remote asymmetric induction.
| Original language | English |
|---|---|
| Pages (from-to) | 6335-6338 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 28 |
| Issue number | 50 |
| DOIs | |
| Publication status | Published - 1987 |
| Externally published | Yes |
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All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry
Cite this
Lactols in stereoselection 1. Highly selective 1,4- and 1,5-asymmetric induction. / Tomooka, Katsuhiko; Okinaga, Tatsuyuki; Suzuki, Keisuke; Tsuchihashi, Gen ichi.
In: Tetrahedron Letters, Vol. 28, No. 50, 1987, p. 6335-6338.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Lactols in stereoselection 1. Highly selective 1,4- and 1,5-asymmetric induction
AU - Tomooka, Katsuhiko
AU - Okinaga, Tatsuyuki
AU - Suzuki, Keisuke
AU - Tsuchihashi, Gen ichi
PY - 1987
Y1 - 1987
N2 - Nucleophilic addition to substituted γ- and δ-lactols with titanium reagents provides 1,4-syn and 1,5-syn diols in high stereoselectivity, which represents a new and simple method for the remote asymmetric induction.
AB - Nucleophilic addition to substituted γ- and δ-lactols with titanium reagents provides 1,4-syn and 1,5-syn diols in high stereoselectivity, which represents a new and simple method for the remote asymmetric induction.
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U2 - 10.1016/S0040-4039(01)91367-X
DO - 10.1016/S0040-4039(01)91367-X
M3 - Article
VL - 28
SP - 6335
EP - 6338
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 50
ER -