Literature DB >> 25882677

Total synthesis of the pseudopterosin aglycones.

Christopher G Newton1, Michael S Sherburn.   

Abstract

The pseudopterosin natural products have been the focus of a substantial number of synthetic studies since the first members were isolated almost 30 years ago. Herein we review all total and formal syntheses of this family of glycosylated diterpenes, with an emphasis on the synthetic strategies employed.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 25882677     DOI: 10.1039/c5np00008d

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  3 in total

1.  Concise Formal Synthesis of the Pseudopterosins via Anionic Oxy-Cope/Transannular Michael Addition Cascade.

Authors:  Vincenzo Ramella; Philipp C Roosen; Christopher D Vanderwal
Journal:  Org Lett       Date:  2020-02-20       Impact factor: 6.005

2.  Broadly Applicable Stereoselective Syntheses of Serrulatane, Amphilectane Diterpenes, and Their Diastereoisomeric Congeners Using Asymmetric Hydrovinylation for Absolute Stereochemical Control.

Authors:  Srinivasarao Tenneti; Souvagya Biswas; Glen Adam Cox; Daniel J Mans; Hwan Jung Lim; T V RajanBabu
Journal:  J Am Chem Soc       Date:  2018-07-27       Impact factor: 15.419

3.  Asymmetric Total Syntheses of Di- and Sesquiterpenoids by Catalytic C-C Activation of Cyclopentanones.

Authors:  Si-Hua Hou; Adriana Y Prichina; Mengxi Zhang; Guangbin Dong
Journal:  Angew Chem Int Ed Engl       Date:  2020-03-12       Impact factor: 15.336

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.