| Abstract: | Treatment of triphenylphosphine with dialkyl acetylenedicarboxylate leads to 1:1 adduct and concomitant protonation of late adduct by pentan‐2,3,4‐trione 3‐oxime gave the reactive intermediate, vinyltriphenylphosphonium salts, which undergoes an intramolecular Wittig reaction to produce tetrasubstituted N‐hydroxypyrroles in fairly high yields. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:100–103, 2008; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20382 |
