Literature DB >> 28152222

Total Synthesis and Stereochemical Assignment of Actinoranone.

Yi-An Guo1, Meng Zhao1, Zhengshuang Xu1, Tao Ye1.   

Abstract

The total synthesis of four actinoranone stereoisomers led to unambiguous assignment of relative and absolute stereochemistry of the natural product. Key features of the convergent, fully stereocontrolled route include the use of a Negishi carbozirconation/iodination, a Friedel-Crafts cyclization, a Felkin-controlled addition reaction, a Mitsunobu reaction, and a late-stage C-H oxidation.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  actinoranone; meroterpenoid; natural products; stereochemistry; total synthesis

Mesh:

Substances:

Year:  2017        PMID: 28152222     DOI: 10.1002/chem.201700476

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  4 in total

1.  Chemoselective Electrosynthesis Using Rapid Alternating Polarity.

Authors:  Yu Kawamata; Kyohei Hayashi; Ethan Carlson; Shobin Shaji; Dirk Waldmann; Bryan J Simmons; Jacob T Edwards; Christoph W Zapf; Masato Saito; Phil S Baran
Journal:  J Am Chem Soc       Date:  2021-10-01       Impact factor: 16.383

2.  Total Synthesis and Structural Reassignment of Laingolide A.

Authors:  Fusong Wu; Tao Zhang; Jie Yu; Yian Guo; Tao Ye
Journal:  Mar Drugs       Date:  2021-04-27       Impact factor: 5.118

Review 3.  Bacterial terpenome.

Authors:  Jeffrey D Rudolf; Tyler A Alsup; Baofu Xu; Zining Li
Journal:  Nat Prod Rep       Date:  2021-05-26       Impact factor: 15.111

4.  Total Synthesis and Biological Evaluation of Kakeromamide A and Its Analogues.

Authors:  Meng Zhao; Yi Xiao; Satoshi Otsuka; Yoichi Nakao; Yian Guo; Tao Ye
Journal:  Front Chem       Date:  2020-05-13       Impact factor: 5.221

  4 in total

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