Literature DB >> 16626159

Efficient and selective reduction protocols of the 2,2-dimethyl-1,3-benzodioxan-4-one functional group to readily provide both substituted salicylaldehydes and 2-hydroxybenzyl alcohols.

Naval Bajwa1, Michael P Jennings.   

Abstract

Two complementary procedures have been developed that selectively allow for the synthesis of either substituted salicylaldehydes or the corresponding 2-hydroxylbenzyl alcohols upon treatment of the 2,2-dimethyl-1,3-benzodioxan-4-one functional group with DIBAL-H or LAH, respectively.

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Year:  2006        PMID: 16626159     DOI: 10.1021/jo0601664

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


  3 in total

1.  Synthesis of functionalized benzo[1,3]dioxin-4-ones from salicylic acid and acetylenic esters and their direct amidation.

Authors:  Rasmi P Bhaskaran; Kalinga H Nayak; Beneesh P Babu
Journal:  RSC Adv       Date:  2021-07-13       Impact factor: 4.036

2.  Total synthesis of the aristolochic acids, their major metabolites, and related compounds.

Authors:  Sivaprasad Attaluri; Charles R Iden; Radha R Bonala; Francis Johnson
Journal:  Chem Res Toxicol       Date:  2014-06-11       Impact factor: 3.739

3.  Efficient preparation of α-ketoacetals.

Authors:  Francisco Ayala-Mata; Citlalli Barrera-Mendoza; Hugo A Jiménez-Vázquez; Elena Vargas-Díaz; L Gerardo Zepeda
Journal:  Molecules       Date:  2012-11-22       Impact factor: 4.411

  3 in total

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