Literature DB >> 12049508

Indium trichloride mediated intramolecular Prins-type cyclization.

Yong Seo Cho1, Hye Yeon Kim, Joo Hwan Cha, Ae Nim Pae, Hun Yeong Koh, Jung Hoon Choi, Moon Ho Chang.   

Abstract

[reaction: see text] Intramolecular Prins-type reactions of compounds having both functionalities of homoallyl alcohol and acetal moiety are described. The intramolecular Prins cyclizations were performed using indium trichloride in chloroform or 25% aqueous THF. Both 9-oxabicyclo[3.3.1]nonane and 3,9-dioxabicyclo[3.3.1]nonane compounds were successfully obtained in moderate yields.

Entities:  

Year:  2002        PMID: 12049508     DOI: 10.1021/ol025856i

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


  1 in total

1.  Evolution of a Strategy for the Enantioselective Total Synthesis of (+)-Psiguadial B.

Authors:  Lauren M Chapman; Jordan C Beck; Caitlin R Lacker; Linglin Wu; Sarah E Reisman
Journal:  J Org Chem       Date:  2018-05-18       Impact factor: 4.354

  1 in total

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