Literature DB >> 12916964

Synthesis of highly substituted 1,3-dienes and 1,3,5-trienes by the palladium-catalyzed coupling of vinylic halides, internal alkynes, and organoboranes.

Xiaoxia Zhang1, Richard C Larock.   

Abstract

[reaction: see text] Highly substituted 1,3-dienes and trienes have been prepared in good to excellent yields by the palladium-catalyzed coupling of vinylic halides, internal alkynes, and organoboranes.

Entities:  

Year:  2003        PMID： 12916964     DOI： 10.1021/ol0348349

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


  2 in total

1.  Design and synthesis of (E)-1-((3-ethyl-2,4,4-trimethylcyclohex-2-enylidene)methyl-4-substituted benzenes from 1-(2,6,6-trimethylcyclohex-1-enyl)ethanol.

Authors:  Bhaskar C Das; Sakkarapalayam M Mahalingam; Todd Evans; George W Kabalka; J Anguiano; K Hema
Journal:  Chem Commun (Camb)       Date:  2009-03-09       Impact factor: 6.222

2.  Stereoselective synthesis of pentasubstituted 1,3-dienes via Ni-catalyzed reductive coupling of unsymmetrical internal alkynes.

Authors:  Zhijun Zhou; Jiachang Chen; Herong Chen; Wangqing Kong
Journal:  Chem Sci       Date:  2020-09-10       Impact factor: 9.825
  2 in total

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