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Facile Synthesis of Saikosaponins.


ABSTRACT: Saikosaponin A (SSa) and D (SSd) are typical oleanane-type saponins featuring a unique 13,28-epoxy-ether moiety at D ring of the aglycones, which exhibit a wide range of biological and pharmacological activities. Herein, we report the first synthesis of saikosaponin A/D (1-2) and their natural congeners, including prosaikosaponin F (3), G (4), saikosaponin Y (5), prosaikogenin (6), and clinoposaponin I (7). The present synthesis features ready preparation of the aglycones of high oxidation state from oleanolic acid, regioselective glycosylation to construct the β-(1→3)-linked disaccharide fragment, and efficient gold(I)-catalyzed glycosylation to install the glycans on to the aglycones.

SUBMITTER: Wang Z 

PROVIDER: S-EPMC8037928 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature

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Facile Synthesis of Saikosaponins.

Wang Ziqiang Z   Wei Bingcheng B   Mu Tong T   Xu Peng P   Yu Biao B  

Molecules (Basel, Switzerland) 20210330 7


Saikosaponin A (SSa) and D (SSd) are typical oleanane-type saponins featuring a unique 13,28-epoxy-ether moiety at D ring of the aglycones, which exhibit a wide range of biological and pharmacological activities. Herein, we report the first synthesis of saikosaponin A/D (<b>1</b>-<b>2</b>) and their natural congeners, including prosaikosaponin F (<b>3</b>), G (<b>4</b>), saikosaponin Y (<b>5</b>), prosaikogenin (<b>6</b>), and clinoposaponin I (<b>7</b>). The present synthesis features ready pre  ...[more]

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