Literature DB >> 29064709

Organocatalytic Phosphonylation of in Situ Formed o-Quinone Methides.

Hai Huang1, Jun Yong Kang1.   

Abstract

A new class of Brønsted acid catalysts based on N-heterocyclic phosphorodiamidic acids (NHPAs) has been developed. The NHPA catalyst promotes phospha-Michael addition reaction of trialkylphosphites to in situ generated ortho-quinone methides (o-QMs) for the construction of diaryl phosphonates in moderate to excellent yields with 1.5 mol % catalyst. Diastereoselective synthesis of P-chiral phosphinate esters is achieved with the use of dialkyl phenylphosphonites.

Entities:  

Year:  2017        PMID: 29064709     DOI: 10.1021/acs.orglett.7b03019

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


  3 in total

1.  Straightforward Synthesis of Bifunctional Phosphorus Phenols via Phosphination of In Situ Generated o-Quinone Methides.

Authors:  Zhangpei Chen; Qinglong Shi; Gongshu Wang; Siwen Chen; Jianshe Hu
Journal:  Molecules       Date:  2018-05-23       Impact factor: 4.411

2.  Enantioselective one-pot synthesis of 4H-chromene derivatives catalyzed by a chiral Ni(ii) complex.

Authors:  Xuan Yu; Wenjie Lan; Jiaqi Li; Hui Bai; Zhaohai Qin; Bin Fu
Journal:  RSC Adv       Date:  2020-12-16       Impact factor: 4.036

3.  Transition-metal-free approach to quinolines via direct oxidative cyclocondensation reaction of N,N-dimethyl enaminones with o-aminobenzyl alcohols.

Authors:  Kairui Rao; Zhangmengjie Chai; Pan Zhou; Donghan Liu; Yulin Sun; Fuchao Yu
Journal:  Front Chem       Date:  2022-09-21       Impact factor: 5.545

  3 in total

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