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Literature DB >> 20602392

Preparation and regioselective Diels-Alder reactions of borylbenzynes: synthesis of functionalized arylboronates.

Takashi Ikawa¹, Akira Takagi, Yurio Kurita, Kozumo Saito, Kenji Azechi, Masahiro Egi, Keisuke Kakiguchi, Yasuyuki Kita, Shuji Akai.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2010 PMID： 20602392 DOI： 10.1002/anie.201002191

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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2 in total

1. Boryl (Hetero)aryne Precursors as Versatile Arylation Reagents: Synthesis through C-H Activation and Orthogonal Reactivity.

Authors: Emilien Demory; Karthik Devaraj; Andreas Orthaber; Paul J Gates; Lukasz T Pilarski
Journal: Angew Chem Int Ed Engl Date: 2015-08-13 Impact factor: 15.336

2. Synthetic studies toward longeracemine: a SmI₂-mediated spirocyclization and rearrangement cascade to construct the 2-azabicyclo[2.2.1]heptane framework.

Authors: Keita Komine; Kyle M Lambert; Quentin R Savage; Joshua B Cox; John L Wood
Journal: Chem Sci Date: 2020-07-30 Impact factor: 9.825

2 in total

Preparation and regioselective Diels-Alder reactions of borylbenzynes: synthesis of functionalized arylboronates.

1. Boryl (Hetero)aryne Precursors as Versatile Arylation Reagents: Synthesis through C-H Activation and Orthogonal Reactivity.

2. Synthetic studies toward longeracemine: a SmI2-mediated spirocyclization and rearrangement cascade to construct the 2-azabicyclo[2.2.1]heptane framework.

2. Synthetic studies toward longeracemine: a SmI₂-mediated spirocyclization and rearrangement cascade to construct the 2-azabicyclo[2.2.1]heptane framework.