// Small Molecule Design & Synthesis Expertise
Professional organic chemistry consulting with 10+ years of experience in medicinal chemistry, custom synthesis, and pharmaceutical route optimization. From concept to commercialization.
// Comprehensive Organic Chemistry Solutions
Design and execute complex multi-step syntheses for pharmaceutical intermediates, natural products, and specialty chemicals. Expert in asymmetric synthesis and stereochemistry control.
Streamline existing synthetic pathways to reduce steps, improve yields, and minimize costs. Process chemistry expertise for scale-up and manufacturing optimization.
Structure-activity relationship analysis and molecular design for drug discovery. Computational chemistry support and retrosynthetic analysis for complex targets.
Comprehensive patent and literature searches. Competitive intelligence and freedom-to-operate analysis. Technical due diligence for pharmaceutical investments.
Scale-up chemistry from laboratory to manufacturing. Process safety evaluation, impurity profiling, and regulatory submission support for pharmaceutical processes.
Technical training for R&D teams. Workshops on modern synthetic methods, reaction mechanisms, and problem-solving strategies in organic chemistry.
// Organic Chemistry PhD with Industrial Experience
// Case Studies & Success Stories
Redesigned a 12-step synthesis route for a cardiovascular drug API, reducing to 6 steps with 45% overall yield improvement and 60% cost reduction. Key improvements included telescoped reactions and elimination of chromatographic purifications.
First asymmetric total synthesis of a marine alkaloid with potent anti-cancer activity. 15-step route featuring innovative cascade cyclization reaction and excellent stereochemical control throughout the sequence.
Designed and synthesized a focused library of 200+ heterocyclic compounds for a kinase inhibitor program, leading to 3 clinical candidates. Structure-activity relationships guided optimization strategy.
Developed environmentally friendly synthesis route replacing toxic reagents and reducing waste by 80% for a diabetes treatment manufacturing process. Achieved same efficiency with safer reagents.
Designed novel chiral auxiliary for enantioselective synthesis of β-amino acids, achieving >95% ee with broad substrate scope and easy recovery. Patent application filed for this innovative methodology.
Developed alternative synthetic routes for blockbuster drug to avoid patent restrictions while maintaining cost-effectiveness for generic manufacturing. Successfully passed regulatory review.
// Ready to Start Your Next Project?