Literature DB >> 32250638

Three-Component Borylallenylation of Alkynes: Access to Densely Boryl-Substituted Ene-allenes.

Shang-Hai Yu1, Tian-Jun Gong1, Yao Fu1.   

Abstract

Ene-allenes serve as versatile building blocks in organic synthesis, and the development of their efficient preparation is valuable. Herein the synthesis of boryl-substituted ene-allenes utilizing a Cu/Pd-catalyzed borylallenylation of alkynes with propargylic carbonates and bis(pinacolato)diboron is reported. Densely (tetra-, penta-, and hexa-) substituted ene-allenes were synthesized in acceptable yield with high regio- and stereoselectivity. More important molecule structures can be obtained by subsequent modifications.

Entities:  

Year:  2020        PMID: 32250638     DOI: 10.1021/acs.orglett.0c00643

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


  3 in total

1.  Cooperative Pd/Cu Catalysis for Alkene Arylboration: Opportunities for Divergent Reactivity.

Authors:  Stanna K Dorn; M Kevin Brown
Journal:  ACS Catal       Date:  2022-01-24       Impact factor: 13.700

2.  Substrate-Controlled Cu(OAc)2-Catalyzed Stereoselective Semi-Reduction of Alkynes with MeOH as the Hydrogen Source.

Authors:  Jiuzhong Huang; Xiaoning Li; Huiling Wen; Lu Ouyang; Nianhua Luo; Jianhua Liao; Renshi Luo
Journal:  ACS Omega       Date:  2021-04-22

3.  Site-Selective (Z)-α-Borylalkenyl Copper Systems for Nucleophilic Stereodefined Allylic Coupling.

Authors:  Mireia Pujol; Ricardo J Maza; Oriol Salvado; Jorge J Carbó; Elena Fernández
Journal:  Angew Chem Int Ed Engl       Date:  2022-08-08       Impact factor: 16.823

  3 in total

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