Autor: |
Graham Walker, Peter J. O'hanlon, Norman H. Rogers, Michael John Crimmin |
Rok vydání: |
1990 |
Předmět: |
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Zdroj: |
ChemInform. 21 |
ISSN: |
0931-7597 |
DOI: |
10.1002/chin.199008331 |
Popis: |
The preparation of a large variety of normonyl heterocycles is described. Methods involving cyclisation of monic acid derivatives gave access to only a limited number of types of heterocycles. Olefination methods proved to be of wider applicability with phosphonate stabilised anions providing the biologically active E-isomer in a 3–4 : 1 excess. The Peterson type olefination proved to be the most useful method with the largest range of heterocycles and stereoselectivity of E:Z 4 to >10 : 1. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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