Literature DB >> 16468726

Palladium-catalyzed multistep reactions involving ring closure of 2-iodophenoxyallenes and ring opening of bicyclic alkenes.

Kanniyappan Parthasarathy1, Masilamani Jeganmohan, Chien-Hong Cheng.   

Abstract

[reaction: see text] An efficient ring closure of 2-iodophenoxy-, 2-iodobenzyloxy-, and 2-iodobenzylaminoallenes followed by ring opening of oxabenzonorbornadienes leading to the synthesis of 2-benzofuranyl, 1H-isochromenyl, or 1,2-dihydroisoquinoline methyl-1,2-dihydro-1-naphthalenol derivatives catalyzed by palladium complexes is described.

Entities:  

Year:  2006        PMID: 16468726     DOI: 10.1021/ol0527936

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


  5 in total

1.  Studies on a urea-directed Stork-Crabtree hydrogenation. Synthesis of the C1-C9 subunit of (+)-zincophorin.

Authors:  Zhenlei Song; Richard P Hsung; Ting Lu; Andrew G Lohse
Journal:  J Org Chem       Date:  2007-11-03       Impact factor: 4.354

2.  Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis.

Authors:  Youran Luo; Álvaro Gutiérrez-Bonet; Jennifer K Matsui; Madeline E Rotella; Ryan Dykstra; Osvaldo Gutierrez; Gary A Molander
Journal:  ACS Catal       Date:  2019-08-28       Impact factor: 13.084

3.  Saucy-Marbet Rearrangements of Alkynyl Halides in the Synthesis of Highly Enantiomerically Enriched Allenyl Halides.

Authors:  Yu Tang; Lichun Shen; Becky J Dellaria; Richard P Hsung
Journal:  Tetrahedron Lett       Date:  2008-11-03       Impact factor: 2.415

4.  Synthesis of amido-spiro[2.2]pentanes via Simmons-Smith cyclopropanation of allenamides.

Authors:  Ting Lu; Ryuji Hayashi; Richard P Hsung; Kyle A DeKorver; Andrew G Lohse; Zhenlei Song; Yu Tang
Journal:  Org Biomol Chem       Date:  2009-06-19       Impact factor: 3.876

Review 5.  Allenamides: a powerful and versatile building block in organic synthesis.

Authors:  Ting Lu; Zhenjie Lu; Zhi-Xiong Ma; Yu Zhang; Richard P Hsung
Journal:  Chem Rev       Date:  2013-04-04       Impact factor: 60.622

  5 in total

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