| Literature DB >> 11271522 |
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