DIAL-A-TERPENE: NEW CHEMICAL PROTOCOLS ALLOWING FOR THE ITERATIVE SYNTHESIS OF TERPENOIDS

Lead Research Organisation: Imperial College London
Department Name: Chemistry

Abstract

Terpenoids, comprised of 'head-to-tail' and 'head-to-head' arrangements of five-carbon atom containing (C5) units, are a very large and diverse class of linear and (poly)cyclic natural occuring biomolecules and account for 60% of known natural products (estimated as more than 40 000 distinct chemical structures). Their vital biological functions include lipid membrane modulation, light harvesting and photooxidative protection, electron transport, intercellular signaling as hormones, and interspecies defence amongst others. Their medicinal benefits have been recognised for centuries, initially as traditional herbal remedies from plants, and subsequent development of e.g., steroidal medicines as blockbuster drugs in the 20th century through to the present day (budesonide was the number 1 prescribed drug of 2013). It is well understood that the (poly)cyclic terpenoids all arise from linear (C5)n precursors, and nature constructs the linear precusors by sequential addition of activated C5 phosphate-containing units. These linear terpenoids are important in their own right, being constituents of nearly every living cell, and play vital roles in peptide modification. A very great deal of chemical, biochemical and biological research has been directed towards the understanding of all of the above, and scientific database searches at the time of writing on "terpen*" (as a catch-all for terpene and terpenoid) reveals > 94 000 manuscripts have been published in this area. However, despite the long-term recognition that these linear compounds are essentially C5-repeating units, a general and iterative chemical protocol for their synthesis - using naturally occuring terpenoid building blocks - does not exist. This is in stark contrast to the state of affairs for synthesis of the other main classes of biologically important compounds (peptides, RNA and oligosaccharides) where use of of solid-phase synthesis, iterative coupling protocols and automated methods has revolutionised these research areas. It is thefore the aim of this proposal to develop such chemical protocols for terpenoids.

Planned Impact

The main purpose of this project is to develop the first general iterative method for the synthesis of terpenes: a key organic chemistry scientific advance and an addition to our knowledge-base. If successful, it will provide a general method for the synthesis of vast numbers of new chemical entities many of which are expected to be pharmaceutically important. These methods may be adopted, adapted and exploited in countless ways by practitioners in academia and in industry for translational research. Since these possibilities are extremely broad - the use of terpenes is an integral and vital part of the cosmetics, fragrance, food, pharmaceutical and biotechnology industries - these many practitioners will undoubtedly be able to see the benefits/applications for/to their own work, and this may lead to wealth creation via the synthesis and application of new chemical entities, which in turn should improve quality of life.
 
Description 1. Tetramethyl Orthosilicate (TMOS) as a Reagent for Direct Amidation of Carboxylic Acids: Tetramethyl orthosilicate (TMOS) is shown to be an effective reagent for direct amidation of aliphatic and aromatic carboxylic acids with amines and anilines. The amide products are obtained in good to quantitative yields in pure form directly after workup without the need for any further purification. A silyl ester as the putative activated intermediate is observed by NMR methods. Amidations on a 1 mol scale are demonstrated with a favorable process mass intensity.

2. A relay cross metathesis reaction has been developed that allows for the iterative synthesis of terpenoids. This is significant since it represents the first iterative method for terpene synthesis using terpenoid building blocks as the reaction partners.
Exploitation Route 1. The TMOS method is a practically convenient synthesis of amides direct from acids and amines and may find multiple applications
2. The Relay cross metathesis (ReXM) method should be applicable to the synthesis of myriad bespoke terpenes
Sectors Chemicals,Manufacturing, including Industrial Biotechology,Pharmaceuticals and Medical Biotechnology

URL http://www.ch.ic.ac.uk/braddock/index.html