Protecting group found for hydroxyls, aminos - Chemical

Postdoctoral fellow student Binghe Wang of the University of Kansas School of Pharmacy told the Division of Organic ... Published online 11 November 2...
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Protecting group found for hydroxyls, aminos

CHICAGO Scientists at the University of Kansas, Lawrence, have devised a reagent to protect hydroxyl and amino groups dur­ ing multistep syntheses. Postdoctoral fel­ low student Binghe Wang of the Univer­ sity of Kansas School of Pharmacy told the Division of Organic Chemistry that the protecting group thus attached is re­ movable by mild reducing agents when no longer wanted. Such a reagent is useful because chemists want to selectively protect groups that are removable by many dif-

ferent mechanisms. Such a choice en­ ables them to apply and remove each group by design, while sparing protect­ ing groups that are still needed. The new reagent is a quinonebutanoic acid, 3-methyl-3-(3,5-dimethyl-2-benzoquinone)butanoic acid. In use, research­ ers would form amides or esters of the carboxyl group. To remove the group, the derivative would be shaken for a few minutes with dilute aqueous sodium dithionite. This procedure reduces the qui­ none to a hydroquinone. A hydroquinone hydroxyl group maneuvers around to displace the amine or alcohol from the carboxyl group to form a coumarin, spe­ cifically 3,4-dihydro-6-hydroxy-4,4^,7-tetramethylcoumarin. The coumarin can be recovered and reoxidized to the quinone reagent. Working with medicinal chemistry professor Ronald T. Borchardt and post­ doctoral fellow Siming Liu, Wang makes the reagent in three steps and in 70% overall yield from commercially avail­ able 2,6-dimethylbenzoquinone.

Protecting group removable by reducing agents

Stephen Stinson

Progress made in design of zeolite synthesis

UÏM.M.NI Researchers haven't yet achieved the ability to design a synthetic route that would make a specific zeolite. But Mark E. Davis, professor of chemical engineering at the California Institute of Technology, Pasadena, believes it won't be long. Davis explored the outlook for zeo­ lite synthesis for the Division of Colloid & Surface Chemistry. Organic struc­ ture-directing agents can be designed, he says, and the required molecular building blocks are available. What re­ mains is to combine these elements with the chemical compatibilities that lead to self-assembly.

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DuPont DBE Intermediates

OH Coumarin derivative X = — O—} - N R R = group being protected, possibly a sugar or amino acid or a natural product

© 1993 DuPont Company

CIRCLE 2 7 ON READER SERVICE CARD SEPTEMBER 13,1993 C&EN

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