Literature DB >> 18027962

Spiroperoxy lactones from furans in one pot: synthesis of (+)-premnalane a.

Ioannis Margaros1, Tamsyn Montagnon, Georgios Vassilikogiannakis.   

Abstract

A [4+2]-cycloaddition between singlet oxygen and a furan, followed by an ene reaction and ketalization, in one synthetic operation, was used for the synthesis of (+)-premnalane A. The first example of a singlet oxygen ene reaction that furnishes exclusively a Z-double bond is noted.

Entities:  

Year:  2007        PMID： 18027962     DOI： 10.1021/ol702575a

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


  3 in total

1.  Synthesis and Characterization of Bimetallic Nanoclusters Stabilized by Chiral and Achiral Polyvinylpyrrolidinones. Catalytic C(sp3)-H Oxidation.

Authors:  Huafang Fan; Zongbo Tong; Zhaoyang Ren; Kanchan Mishra; Shunya Morita; Edruce Edouarzin; Lingaraju Gorla; Boris Averkiev; Victor W Day; Duy H Hua
Journal:  J Org Chem       Date:  2022-05-05       Impact factor: 4.198

Review 2.  Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products.

Authors:  Alexander O Terent'ev; Dmitry A Borisov; Vera A Vil'; Valery M Dembitsky
Journal:  Beilstein J Org Chem       Date:  2014-01-08       Impact factor: 2.883

3.  Crystal structure of 3a,6,6,9a-tetra-methyl-dodeca-hydro-naphtho-[2,1-b]furan-2-ol.

Authors:  Xin-Wei Shi; Sheng-Kun Li; Dang-Dang Li; Qiang-Qiang Lu
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2015-09-12
  3 in total

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