Controlling the building blocks of life

Dec 10, 2008
Controlling the building blocks of life

(PhysOrg.com) -- A simple and reliable method for converting one of the simplest chemical entities into one of the most difficult-to-make molecular building blocks of life, with complete control over its shape, is reported by scientists at the University of Bristol in this week's Nature [11 December].

It will have major implications for the synthesis of drugs and agrochemicals.

Many important molecules required for life exist in two forms that are mirror images of each other – like our left and right hands. This property is called ‘chirality’, from the Greek word for hand, and the two forms are called ‘enantiomers’, from the Greek word for opposite.

The classic example of the drug thalidomide illustrates the difference in biological response to chiral molecules: one of the two enantiomers caused devastating birth defects, whereas its mirror image had the desired sedative properties that doctors’ prescribed it for.

Since this catastrophe, and the subsequent recognition of the importance of the relationship between a small molecule (for example a drug) and its site of action (for example a protein), it has become necessary to test individual enantiomers and not mixtures of the two forms. But a mixture of enantiomers can be very difficult to separate.

Professor Varindar Aggarwal at the University of Bristol has now developed a simple and reliable method for converting one of the simplest chemical entities into one of the most difficult-to-make molecular building blocks of life, with complete control over its shape.

Professor Aggarwal explained the importance of this work: “We live in a chiral world. Indeed, chirality and life are so inextricably linked that the detection of chirality outside our planet is used as a test for extraterrestrial life.

“It is the shape and function of a molecule that gives rise to its properties. For example, the different smell of oranges and lemons comes from two molecules, identical except for their three-dimensional spatial arrangement. Thus being able to control the shape and function of enantiomers is critical to the many applications of organic chemical synthesis.”

This work is likely to find broad application in the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals where such difficult shapes are often encountered.

Aggarwal and colleagues have developed a two-step process that can be used to convert readily available secondary alcohols into single mirror image forms of tertiary alcohols that contain a quaternary stereogenic centre (a carbon atom with four different non-hydrogen substituents). Either mirror image of the tertiary alcohol can be made with very high levels of control over its shape.

Provided by University of Bristol

Explore further: Building the ideal rest stop for protons

add to favorites email to friend print save as pdf

Related Stories

Getting a grip on robotic grasp

Jul 18, 2014

Twisting a screwdriver, removing a bottle cap, and peeling a banana are just a few simple tasks that are tricky to pull off single-handedly. Now a new wrist-mounted robot can provide a helping hand—or rather, ...

New tool, savings for manufacturing hard materials

Jul 17, 2014

"Machining," in particular the process of cutting hard, brittle materials during manufacturing, can be difficult, often because the cutting tool, typically made of single crystal diamond, the hardest material ...

Recommended for you

Building the ideal rest stop for protons

6 hours ago

Where protons, or positive charges, decide to rest makes the difference between proceeding towards ammonia (NH3) production or not, according to scientists at Pacific Northwest National Laboratory (PNNL) and ...

Cagey material acts as alcohol factory

8 hours ago

Some chemical conversions are harder than others. Refining natural gas into an easy-to-transport, easy-to-store liquid alcohol has so far been a logistic and economic challenge. But now, a new material, designed ...

User comments : 0