Literature DB >> 34791884

Studies toward the Total Syntheses of Calyciphylline D-Type Daphniphyllum Alkaloids.

Yi Cui1, Jun Ren1, Jiayuan Lv1, Zhongwen Wang1.   

Abstract

An efficient construction of an aza-[5.7.6.5] tetracyclic core structure of calyciphylline D-type Daphniphyllum alkaloids has been achieved. The synthetic route features a diastereoselective cyclopropanation, efficient construction of the core bridged 8-aza-[3.2.1]octane skeleton through a [3 + 2] IMCC strategy, oxidative dearomatization of phenol, and gram-scale preparation in each step.

Entities:  

Year:  2021        PMID: 34791884     DOI: 10.1021/acs.orglett.1c03497

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


  1 in total

1.  Highly efficient construction of an oxa-[3.2.1]octane-embedded 5-7-6 tricyclic carbon skeleton and ring-opening of the bridged ring via C-O bond cleavage.

Authors:  Yi Cui; Jiayuan Lv; Tianhang Song; Jun Ren; Zhongwen Wang
Journal:  RSC Adv       Date:  2022-03-25       Impact factor: 3.361

  1 in total

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