C-Heteroatom Bond Formation In Lewis Acid Catalysed Allylic Substitution Reaction
2013
Liene Grigorjeva

Defending
04.10.2013. 14:00, Materiālzinātnes un lietišķās ķīmijas fakultāte, Āzenes ielā 14/24, 272.telpa

Supervisor
Aigars Jirgensons

Reviewers
Raimonds Valters, Māris Turks, Mārtiņš Katkevičs

A novel method for the synthesis of unsaturated amino alcohols and amino acids, as well as C-quaternary vinylglycinols has been developed. A convenient approach to 2-trichloromethyl-4-vinyloxazoline and its ring cleavage reactions with various nucleophiles have been demonstrated. Novel approach for the synthesis of N-tosyliminocarbonates has been established their synthetic application was demonstrated. The thesis is presented as a set of thematically unified scientific publications on C-heteroatom bond formation in Lewis acid catalysed nucleophilic allylic substitution of trichloroacetimidate group. It consists of 4 publications in peer-reviewed journals that are included in international scientific databases and 1 manuscript. The publications are written in English and constitute a total of 34 pages.


Keywords
NUCLEOPHILIC SUBSTITUTION, CYCLIZATION, LEWIS ACID CATALYSIS, C-N AND C-O BOND FORMATION

Grigorjeva, Liene. C-Heteroatom Bond Formation In Lewis Acid Catalysed Allylic Substitution Reaction. PhD Thesis. Rīga: [RTU], 2013. 34 p.

Publication language
Latvian (lv)
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