Dimerization approach to (+)-asperazine A
Tryptophan-linked dimeric diketopiperazine alkaloids possess great molecular diversity and bioactivity. In this issue of Chem, Jiang and co-workers report an oxidative approach to those alkaloids containing an unsymmetrical C3-N1′ linkage. In their concise synthesis of (+)-asperazine, they successfu...
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Published in | Chem Vol. 9; no. 2; pp. 258 - 259 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
09.02.2023
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Online Access | Get full text |
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Summary: | Tryptophan-linked dimeric diketopiperazine alkaloids possess great molecular diversity and bioactivity. In this issue of Chem, Jiang and co-workers report an oxidative approach to those alkaloids containing an unsymmetrical C3-N1′ linkage. In their concise synthesis of (+)-asperazine, they successfully dimerized a designer tryptophan-alternative building block through the sustained release of electrophilic iodine.
Tryptophan-linked dimeric diketopiperazine alkaloids possess great molecular diversity and bioactivity. In this issue of Chem, Jiang and co-workers report an oxidative approach to those alkaloids containing an unsymmetrical C3-N1′ linkage. In their concise synthesis of (+)-asperazine, they successfully dimerized a designer tryptophan-alternative building block through the sustained release of electrophilic iodine. |
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ISSN: | 2451-9294 2451-9294 |
DOI: | 10.1016/j.chempr.2023.01.015 |