Literature DB >> 18681405

Controllable one-step synthesis of spirocycles, polycycles, and di- and tetrahydronaphthalenes from aryl-substituted propargylic alcohols.

Wen Huang1, Pengzhi Zheng, Zhengxing Zhang, Ruiting Liu, Zhenxia Chen, Xigeng Zhou.   

Abstract

A novel, convenient, and efficient method has been developed for selective synthesis of spirocycle, polycycle, and di- and tetrahydronaphthalene systems from aryl-substituted propargylic alcohols by FeCl3- or TsOH-catalyzed multiple activations of unsaturated C-C bonds and C-H bonds.

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Year:  2008        PMID: 18681405     DOI: 10.1021/jo801210n

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

Review 1.  Scope and advances in the catalytic propargylic substitution reaction.

Authors:  Rashmi Roy; Satyajit Saha
Journal:  RSC Adv       Date:  2018-09-05       Impact factor: 3.361

2.  Preparation of an advanced intermediate for the synthesis of leustroducsins and phoslactomycins by heterocycloaddition.

Authors:  Anaïs Rousseau; Guillaume Vincent; Cyrille Kouklovsky
Journal:  Beilstein J Org Chem       Date:  2022-10-04       Impact factor: 2.544

  2 in total

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