Synthetic Routes to Methylerythritol Phosphate Pathway Intermediates and Downstream Isoprenoids

Title:Synthetic Routes to Methylerythritol Phosphate Pathway Intermediates and Downstream Isoprenoids

Volume: 18 Issue: 8

Author(s): Sarah K. Jarchow-Choy, Andrew T. Koppisch and David T. Fox

Affiliation:

Keywords: Enzyme mechanism, isoprenoids, terpenes, MEP pathway.

Abstract: Isoprenoids constitute the largest class of natural products with greater than 55,000 identified members. They play essential roles in maintaining proper cellular function leading to maintenance of human health, plant defense mechanisms against predators, and are often exploited for their beneficial properties in the pharmaceutical and nutraceutical industries. Most impressively, all known isoprenoids are derived from one of two C₅-precursors, isopentenyl diphosphate (IPP) or dimethylallyl diphosphate (DMAPP). In order to study the enzyme transformations leading to the extensive structural diversity found within this class of compounds there must be access to the substrates. Sometimes, intermediates within a biological pathway can be isolated and used directly to study enzyme/pathway function. However, the primary route to most of the isoprenoid intermediates is through chemical catalysis. As such, this review provides the first exhaustive examination of synthetic routes to isoprenoid and isoprenoid precursors with particular emphasis on the syntheses of intermediates found as part of the 2C-methylerythritol 4-phosphate (MEP) pathway. In addition, representative syntheses are presented for the monoterpenes (C₁₀), sesquiterpenes (C₁₅), diterpenes (C₂₀), triterpenes (C₃₀) and tetraterpenes (C₄₀). Finally, in some instances, the synthetic routes to substrate analogs found both within the MEP pathway and downstream isoprenoids are examined.

Cite this article as:

Jarchow-Choy K. Sarah, Koppisch T. Andrew and Fox T. David, Synthetic Routes to Methylerythritol Phosphate Pathway Intermediates and Downstream Isoprenoids, Current Organic Chemistry 2014; 18 (8) . https://dx.doi.org/10.2174/1385272819666140501001101