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        <datestamp>2026-09-30T16:27:38Z</datestamp>
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          <dc:title>Transition-Metal-Free
Regioselective Construction
of Cyano- and Phosphonyl Tetrazole Derivatives</dc:title>
          <dc:creator>Yufeng Wang (274657)</dc:creator>
          <dc:creator>Zeya Xu (10921395)</dc:creator>
          <dc:creator>Ruiqi Liu (3873832)</dc:creator>
          <dc:creator>Yuting Zheng (2176086)</dc:creator>
          <dc:creator>Jia Zhou (53252)</dc:creator>
          <dc:creator>Xiaoran Chen (11616265)</dc:creator>
          <dc:creator>Tingpu Guo (25144899)</dc:creator>
          <dc:creator>Yulei Zhao (3129630)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Sociology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>phosphonyl tetrazole derivatives</dc:subject>
          <dc:subject>precious metal catalysts</dc:subject>
          <dc:subject>free regioselective construction</dc:subject>
          <dc:subject>substituted tetrazoles</dc:subject>
          <dc:subject>scale reactions</dc:subject>
          <dc:subject>regioselective synthesis</dc:subject>
          <dc:subject>promising applications</dc:subject>
          <dc:subject>product transformation</dc:subject>
          <dc:subject>nearly ineffective</dc:subject>
          <dc:subject>natural products</dc:subject>
          <dc:subject>enhances safety</dc:subject>
          <dc:subject>dual tetrazoles</dc:subject>
          <dc:subject>brønsted base</dc:subject>
          <dc:subject>arylazo sulfones</dc:subject>
          <dc:subject>also avoids</dc:subject>
          <dc:description>A Brønsted base-promoted, transition-metal-free
[3 + 2] cycloaddition
for the regioselective synthesis of cyano- and phosphonyl-substituted
tetrazoles is reported. Compared to readily decomposing diazonium
salts, the use of arylazo sulfones not only enhances safety but also
avoids the need for precious metal catalysts. Arylazo sulfones exhibit
excellent reactivity, whereas other commonly used azo compounds are
nearly ineffective. Modification of natural products, synthesis of
dual tetrazoles, gram-scale reactions, and investigations into product
transformation further highlight the promising applications.</dc:description>
          <dc:date>2026-09-30T00:00:00Z</dc:date>
          <dc:type>Text</dc:type>
          <dc:type>Journal contribution</dc:type>
          <dc:identifier>10.1021/acs.joc.6c01824.s001</dc:identifier>
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