[2 + 2 + 2]Cycloaddition Reaction of 1-Methylpyrrole with Diethyl Azodicarboxylate

  • Lee, Chang-kiu
  • Ahn, Yu-mi
Citations

SCOPUS

4

초록

Reactions of bimolecular [2 + 2 + 2] cycloaddition are of interest since they serve as examples of orbital interactions that can be explained by the Woodward-Hoffmann rules.1 However, concerted [2 + 2 + 2] cycloadditions involving three molecules are rare. For example, trimerization of acetylene to benzene needs a catalyst such as A1C1<inf>3</inf> and a 1:1 adduct is involved in the course of formation, indicating a stepwise process.2 Although few reports are found in the literature, termolecular [2 + 2 + 2] cycloaddition reactions seem to be useful synthetic processes if a suitable catalyst is employed.3-7We report an example of an uncatalyzed cycloaddition reaction that appears to involve 6 π electrons from three double bonds in three molecules. © 1990, American Chemical Society. All rights reserved.

제목
[2 + 2 + 2]Cycloaddition Reaction of 1-Methylpyrrole with Diethyl Azodicarboxylate
저자
Lee, Chang-kiuAhn, Yu-mi
DOI
10.1021/jo00299a049
발행일
1990
유형
Article
저널명
The Journal of Organic Chemistry
55
12
페이지
3957 ~ 3958