Abstract
The diastereoselectivity on addition of γ‐substituted allylboronates to α‐methylbutyraldehyde (9) did not depend on the size of the substitutent in the reagent, but only on its location in the Z or E position. This finding required a reinterpretation of the reasons for the attendant reversal in diastereoselectivity. New hypotheses are presented based on force‐field calculations on model structures for the transition states.
Original language | English |
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Pages (from-to) | 2387-2394 |
Number of pages | 8 |
Journal | Chemische Berichte |
Volume | 123 |
Issue number | 12 |
DOIs | |
State | Published - 1990 |
Externally published | Yes |
Keywords
- Allylboration reaction
- Calculations, force‐field
- Transition‐state models