Literature DB >> 33481616

Radical trans-Hydroboration of Substituted 1,3-Diynes with an N-Heterocyclic Carbene Borane.

Kosuke Takahashi, Steven J Geib1, Katsuhiro Maeda, Dennis P Curran1, Tsuyoshi Taniguchi.   

Abstract

Monohydroboration of substituted 1,3-diynes with an N-heterocyclic carbene borane (NHC-borane) occurs under radical conditions using an azo initiator, such as ACCN and AIBN, and a thiol as a polarity-reversal catalyst. The reaction is highly regio- and stereoselective and provides stable NHC-(E)-alkynylalkenylboranes.

Entities:  

Year:  2021        PMID: 33481616     DOI: 10.1021/acs.orglett.0c04284

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


  2 in total

1.  Photoinduced successive oxidative ring-opening and borylation of indolizines with NHC-boranes.

Authors:  Huitao Zheng; Honggang Xiong; Chaobo Su; Hua Cao; Huagang Yao; Xiang Liu
Journal:  RSC Adv       Date:  2021-12-21       Impact factor: 3.361

2.  Stereoselective hydrogen atom transfer to acyclic radicals: a switch enabling diastereodivergent borylative radical cascades.

Authors:  Tian Ye; Feng-Lian Zhang; Hui-Min Xia; Xi Zhou; Zhi-Xiang Yu; Yi-Feng Wang
Journal:  Nat Commun       Date:  2022-01-20       Impact factor: 17.694

  2 in total

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