期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 16, 期 9, 页码 1519-1526出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob03047a
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资金
- Ministere de l'enseignement superieur et de la recherche
- Ministere des affaires etrangeres et du developpement international
- Ministry of Higher Education, Scientific Research, and Technology of Tunisia
The successive addition of two different Grignard reagents to acyl cyanohydrins was performed with success by taking advantage of the low reactivity of alkynyl Grignard reagents. The experimental conditions were adjusted so that they were not reactive during the first addition step, but reactive only in the second one. The synthetic utility of the prepared compounds was validated by the preparation of chiral quaternary alpha-amino acids.
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