Abstract
Iodocarbocyclization reactions of dimethyl alkenylmalonates in the presence of I2 and Ti(Ot-Bu)4 proceed in a regioselective and stereospecific manner through an ionic mechanism.
Original language | English |
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Pages (from-to) | 2167-2170 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 33 |
Issue number | 16 |
DOIs | |
Publication status | Published - 1992 Apr 14 |
Externally published | Yes |
Keywords
- alkenylmalonate
- cyclopentane derivative
- iodine
- iodocarbocyclization
- γ-butyrolactone
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry