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Monday, 23 May 2016

Elvira Haimov

Elvira Haimov

Elvira Haimov

Postdoctoral Fellow at Technion - Israel Institute of Technology

links
https://il.linkedin.com/in/elvira-haimov-1207a031
https://www.facebook.com/elvira.haimov
https://plus.google.com/102948504361920012718/about




Experience

Postdoctoral Fellow

Technion - Israel Institute of Technology
– Present (5 months)
During my postdoctoral fellowship at the group of Prof. Dr. Ilan Marek I was in charge of projects invited by the industry, managing to upgrade them to the desired level, in limited time schedule.

Direct Ph.D in Organic Chemistry.

Technion - Israel Institute of Technology
(3 years 10 months)haifa
During my doctoral studies I was developing new methodologies in Organic Synthesis, under the title - "Stereoselective synthesis of enolate intermediate toward the construction of quaternary stereocenters". I gained experience in frontal teaching in advanced Organic Chemistry course.

MSc Student in Organic Chemistry at the Faculty of Chemistry

Technion - Israel Institute of Technology
(2 years)Israel
During my Msc studies I was responsible for method development in Organic Chemistry under the subject of "Synthesis of Polyhydroxylated Fragments toward natural products" and teaching undergraduate students.

Research Assistant at Stereoselective OrganoChemistry Laboratory at the Faculty of Chemistry at the

Technion - Israel Institute of Technology
(1 year)
While experiencing the Organic Chemistry laboratory as a research assistant I was handling various techniques and systems in Organic Chemistry and performing wide range of reactions.

 Elvira Haimov

Education

Organizations

Israel Chemical Society

Starting

Publications

Stereoselective Formation of Fully Substituted Ketone Enolates(Link)

2016
March 2016
Our approach leading to the formation of several new stereogenic centers through a combined metalation–addition of a carbonyl–carbamoyl transfer to reveal in situ stereodefined α,α-disubstituted enolates of ketone as a single stereoisomer. This approach could produce a series of aldol and Mannich products from enol carbamate with excellent diastereomeric ratios.

 

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