Volume 90 Issue 27 | p. 9 | News of The Week
Issue Date: July 2, 2012 | Web Date: June 29, 2012

Reaching For Meta Substitution

Catalysis: C–H activation strategy might aid challenging problems in synthesis
Department: Science & Technology | Collection: Green Chemistry
Keywords: Organometallic chemistry, palladium, C-H activation, meta-substitution, aromatic
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STRAIN RELIEF
A nitrile template (red) directs C–H activation to the meta position of arenes.
A reaction scheme showing meta substitution using a palladium catalyst.
 
STRAIN RELIEF
A nitrile template (red) directs C–H activation to the meta position of arenes.

A new mode of C–H activation selectively functionalizes the meta position of aromatic rings, chemists at Scripps Research Institute report (Nature, DOI: 10.1038/nature11158). The strategy could make it easier to bring C–H activation to bear on challenging problems in synthesis, including making drugs with sophisticated substitution patterns.

Despite advances in the activation of inert C–H bonds, it’s still tough to selectively transform one C–H bond among many in an aromatic ring. Chemists’ typical solution is a directing group, which tends to form a rigid six- or seven-membered ring transition state with a metal catalyst and produces ortho-substituted products. Meta substitution has remained elusive because it would require a larger ring called a cyclophane in the transition state, which would be strained.

Jin-Quan Yu, postdoctoral researchers Dasheng (Jackson) Leow and Gang Li, and graduate student Tian-Sheng (Tyson) Mei realized they could relieve that strain by designing a less-rigid transition state. They devised a nitrile template that coordinates weakly to a palladium catalyst in an “end-on” fashion yet is reactive enough to overcome the entropy in a floppy transition state.

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WEAK IS GOOD
The Yu team’s removable template coordinates weakly to Pd and overrides the intrinsic electronic and steric properties of arene substrates. Bulky alkyl groups (R) ensure that the nitrile, substrate, and Pd align for optimum reactivity.
A structure of a palladium template used in meta substitution.
 
WEAK IS GOOD
The Yu team’s removable template coordinates weakly to Pd and overrides the intrinsic electronic and steric properties of arene substrates. Bulky alkyl groups (R) ensure that the nitrile, substrate, and Pd align for optimum reactivity.

The result is meta functionalization of a variety of toluene derivatives. Adjusting the nitrile template makes it possible to modify hydrocinnamic acid derivatives, which are structural motifs in the multiple myeloma drug Velcade and the blood-pressure-lowering drug Micardis. After the transformation, the team removes the templates through reduction or hydrolysis reactions. The template idea is flexible, Yu says, and it should be adaptable for a wide variety of arenes, including phenols.

Outside C–H activation, some methods for meta functionalization do exist, explains Victor A. Snieckus of Queens University, who has written a commentary about the work (Nature, DOI: 10.1038/486478a). However, meta substitution on electron-rich aromatic rings remains “a tricky business,” he adds. “Yu’s work offers an intriguing coordination-driven method for selective meta activation,” but the templates will need to be reduced in both size and complexity to make the technique broadly usable, he says.

“This is an interesting and creative strategy,” says Melanie S. Sanford, whose University of Michigan, Ann Arbor, team develops directed C–H activation methods. In the C–H activation realm, meta functionalization “has proven very, very hard to do in any type of general sense previously, because directing groups are almost universally ortho selective,” she explains. “The selectivity for the meta position is not yet perfect, but this looks like a very promising start.”

 
Chemical & Engineering News
ISSN 0009-2347
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Comments
Kishor Inamke (Sun Jul 01 03:42:41 EDT 2012)
Its very very interesting. Need to focus on other ortho
Activating group.. Impressive.

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