Literature DB >> 11271522

Highly efficient synthesis of linear pyrrole oligomers by twofold Heck reactions.

L F Tietze1, G Kettschau, U Heuschert, G Nordmann.   

Abstract

The twofold Heck reaction of the vinylpyrroles 3a and 3b with the iodobenzenes 4a-c led to the linear pyrrole oligomers 5, 6, and 7. The synthesis of both symmetrical and unsymmetrical oligomers, such as 10a and 10b, was also accomplished by a Heck reaction of 8 and 9 and by a Heck reaction of 3a and 11 followed by a Wittig reaction and a second Heck reaction with 8. The pentacyclic oligomers 14 and 19 were prepared by a twofold Heck reaction of 13 with 4 and by a twofold Heck reaction of 15 with 16 followed by a Wittig reaction and a twofold Heck reaction with 8.

Entities:  

Year:  2001        PMID: 11271522     DOI: 10.1002/1521-3765(20010119)7:2<368::aid-chem368>3.0.co;2-2

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Mizoroki-heck cross-coupling reactions catalyzed by dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium under mild reaction conditions.

Authors:  Miriam Oberholzer; Christian M Frech
Journal:  J Vis Exp       Date:  2014-03-20       Impact factor: 1.355

Review 2.  Applications of SBA-15 supported Pd metal catalysts as nanoreactors in C-C coupling reactions.

Authors:  Ghodsi Mohammadi Ziarani; Sahar Rohani; Abolfazl Ziarati; Alireza Badiei
Journal:  RSC Adv       Date:  2018-12-07       Impact factor: 4.036

  2 in total

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