Literature DB >> 24666217

Ivorenolide B, an immunosuppressive 17-membered macrolide from Khaya ivorensis: structural determination and total synthesis.

Yao Wang1, Qun-Fang Liu, Ji-Jun Xue, Yu Zhou, Huang-Chao Yu, Sheng-Ping Yang, Bo Zhang, Jian-Ping Zuo, Ying Li, Jian-Min Yue.   

Abstract

Ivorenolide B (1), an unprecedented 17-membered macrolide featuring conjugated acetylenic bonds and four chiral centers, was isolated from Khaya ivorensis. The structure of 1 was fully determined by spectroscopic analysis and total syntheses of its four most possible stereoisomers. Compound 1 showed significant immunosuppressive activity.

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Year:  2014        PMID: 24666217     DOI: 10.1021/ol500667d

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Synthesis of 1,3-Diynes via Cadiot-Chodkiewicz Coupling of Volatile, in Situ Generated Bromoalkynes.

Authors:  Phil C Knutson; Haleigh E Fredericks; Eric M Ferreira
Journal:  Org Lett       Date:  2018-10-17       Impact factor: 6.005

2.  Synthesis and biological activities of petrosiols B and D.

Authors:  Jialin Geng; Qidong Ren; Caizhu Chang; Xinni Xie; Jun Liu; Yuguo Du
Journal:  RSC Adv       Date:  2019-04-01       Impact factor: 3.361

  2 in total

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