Synthetic Chemist

Yevhenii Vaiser

Bridged nitrogen scaffolds for drug discovery.
3.5 years at Enamine Ltd. — seeking an MSc position in Germany.

Yevhenii Vaiser

About

I am a synthetic chemist with 3.5 years of professional experience at Enamine Ltd., Kyiv — one of the world's largest suppliers of screening compounds and building blocks for drug discovery. My work spans the full scale range, from milligram-level discovery synthesis to kilogram production, with a focus on bridged aliphatic scaffolds, particularly azabicyclic compounds of interest to medicinal chemistry programs globally.

My BSc thesis, completed in collaboration with Enamine and Taras Shevchenko National University of Kyiv, introduced a novel synthetic route to 1,4-difunctionalized 7-azabicyclo[2.2.1]heptanes via sequential directed bridgehead lithiation — earning a score of 98/100. I subsequently took part in the Mitacs Globalink Research Internship at the University of Regina, Canada, where I investigated the synthesis of twisted polycyclic aromatic hydrocarbons through α-allylation strategies.

I am looking for an MSc position in Germany in organic or medicinal chemistry — ideally in a group working on synthesis methodology, scaffold design, or drug discovery-oriented chemistry. My long-term goal is a career in the European pharmaceutical industry or academic research.

Outside of work Hiking · Reading · Chess

Research

Thesis 2024 – 2025

A Novel Approach to the Synthesis of 1,4-Difunctionalized 7-Azabicyclo[2.2.1]heptanes

Taras Shevchenko National University of Kyiv KNUEnamine Ltd. 98 / 100

Supervisor: Kyrychok O. O.

Developed a new synthetic route to 7-azabicyclo[2.2.1]heptane building blocks bearing functional groups at both bridgehead positions (C-1 and C-4). The key strategy employs sequential directed lithiation (sec-BuLi) of bridgehead carbons followed by electrophilic quench (CO₂), starting from commercially available trans-4-(Boc-amino)cyclohexanol. The protocol delivers quantitative yields and enables access to scaffolds relevant to drug discovery — including epibatidine analogues and nAChR ligands.

Internship Summer – Fall 2025

Synthesis of Twisted Polycyclic Aromatic Hydrocarbons through α-Allylation

University of Regina, Canada Mitacs Globalink

Supervisor: Prof. Marc MacKinnon

Research internship funded by the Mitacs Globalink program. Investigated the synthesis of non-planar twisted PAH frameworks via α-allylation strategies under the supervision of Prof. Marc MacKinnon. Completed October 2025.

Conference 2025

Modern Problems of Chemistry — Annual Conference, KNU (2025)

Taras Shevchenko National University of Kyiv Organic Chemistry section

Presented original research on the synthesis of 1,4-difunctionalized 7-azabicyclo[2.2.1]heptanes at the international student and postgraduate conference of the Chemistry Faculty. Conference page: conf.chem.knu.ua.

Experience

Enamine Ltd.

One of the world's largest suppliers of screening compounds and building blocks for drug discovery. Synthetic Chemist
  • Design, synthesis, and scale-up of building blocks for pharmaceutical chemistry across milligram to kilogram scales
  • Specialization in bridged aliphatic scaffolds — azabicyclic compounds relevant to drug discovery
  • Contracted FTE chemist on an R&D collaboration with a major pharmaceutical partner (~1.5 years)
  • Applied directed metalation chemistry (sec-BuLi), protecting group strategies (Boc, TBS), and functional group transformations
  • Quality control at all synthetic stages; maintained ELN records in Signals Notebook
  • Supervised a student intern during the final three months

Education

Taras Shevchenko National University of Kyiv

BSc Chemistry · Chemistry · Organic Chemistry
2021 – 2025
UA Weighted Avg
83.9 / 100
DE · Bayerische Formel
2.19 Gut
US GPA · WES Standard
2.91 / 4.0 · B
240 ECTS Thesis: 98/100 Final exam: 91/100

Graduated June 2025. Thesis developed in collaboration with Enamine Ltd.

Notable Coursework

Organic Chemistry 96 10 ECTS
Organic Chemistry (aromatic & heterocyclic) 90 6 ECTS
Mechanisms of Organic Reactions 79 3 ECTS
Stereochemistry of Organic Compounds 87 3 ECTS
General Stereochemistry 94 4 ECTS
Asymmetrical Synthesis 76 3 ECTS
Selected Sections of Organic Chemistry 80 5 ECTS
Chemistry of Heterocyclic Compounds 90 3 ECTS
Fundamentals of Analytical Chemistry 77 11 ECTS
Instrumental Methods of Analysis 79 9 ECTS
Physical Methods of Analysis in Chemistry 80 9 ECTS
Chromatographic Methods in Organic Chemistry 82 5 ECTS
Functional and Elemental Analysis 85 4 ECTS
Physical Chemistry 75 9 ECTS
Physical Chemistry of Processes 79 9 ECTS
Quantum Chemistry 64 4 ECTS
Colloid Chemistry 78 5 ECTS
General Chemistry 88 7 ECTS
Inorganic Chemistry 90 7 ECTS
Crystal Chemistry 90 4 ECTS
Chemistry of Transitional Elements 90 6 ECTS
Organic Materials 78 3 ECTS
Polymer Science 79 8 ECTS
Technology of Production (Organic & Polymers) 85 4 ECTS
Molecular Biology 87 3 ECTS
Modern Medicines 87 4 ECTS
Protein Chemistry 68 3 ECTS
Chemistry of Biomolecules and Bioprocesses 70 4 ECTS
Research Practice 96 6 ECTS
Bachelor's Qualification Work 98 6 ECTS
Physics 85 12 ECTS
Advanced Mathematics 98 10 ECTS
Statistic Methods 95 3 ECTS
Information Technology in Chemistry 100 4 ECTS
Modern Software in Chemistry / Teaching Practice 84 2 ECTS
Ecology 90 2 ECTS
History of Chemistry 93 3 ECTS
Foreign Language 76 17 ECTS
Philosophy 75 4 ECTS
Ukrainian and Foreign Culture 81 3 ECTS
Social and Political Studies 93 2 ECTS
Rhetoric 90 3 ECTS
Pedagogy 91 3 ECTS
Introduction into University Studios 85 2 ECTS
Jurisprudence & Entrepreneurial Activity 69 3 ECTS

Skills

Synthetic

Multi-step synthesisDirected metalationProtecting groups (Boc, TBS)FG transformationsBridged scaffoldsAzabicyclic compoundsBuilding block synthesis

Analytical

HPLCLC-MSGC-MSNMR (1D / 2D)TLC

Software

ChemDrawMestReNovaSignals Notebook (ELN)ReaxysISIS/Symyx DrawMendeleyMS Office

Languages

Ukrainian C2
A1 A2 B1 B2 C1 C2
English C1
TOEFL iBT 110/120 · March 2026
A1 A2 B1 B2 C1 C2
German A2
Actively learning
A1 A2 B1 B2 C1 C2

Get In Touch

I am open to MSc opportunities in Germany and to conversations with research groups working in organic or medicinal chemistry. Feel free to reach out by email.

evaiser2004@gmail.com Download CV