Concepedia

Chemoenzymatic Synthesis of the Microbial Elicitor (−)-Syringolide via a Fructose 1,6-Diphosphate Aldolase-Catalyzed Condensation Reaction

Robert Chênevert, Mohammed Dasser

The Journal of Organic Chemistry · 2000 · 34 citations · 18 references

DOI

Concepts

Abstract

Syringolide 2, an elicitor of the bacterial plant pathogen Pseudomonas syringae pv. tomato which triggers a hypersensitive defense response in resistant soybean plants, has been synthesized in five steps via a fructose 1,6-diphosphate aldolase reaction.

References

18

Meldrum's acid in organic synthesis. 2. A general and versatile synthesis of .beta.-keto esters

Yuji Oikawa, Kiyoshi Sugano, Osamu Yonemitsu · The Journal of Organic Chemistry · 1978 · 301 citations

, , +4

The structures of syringolides 1 and 2, novel C-glycosidic elicitors from Pseudomonas syringae pv. tomato

Sharon L. Midland, Noel T. Keen, James J. Sims et al. · The Journal of Organic Chemistry · 1993 · 107 citations

, , +9

An Efficient Multigram-Scale Preparation of Dihydroxyacetone Phosphate

Sang‐Hun Jung, Jin-Hyun Jeong, Paula C. Miller et al. · The Journal of Organic Chemistry · 1994 · 73 citations

, , +5

Enantioselective Syntheses of Syributin 1 and Novel C-Glycosidic Elicitors Syringolides 1 and 2

Toshio Honda, Hirotake Mizutani, Kazuo Kanai · The Journal of Organic Chemistry · 1996 · 48 citations

, , +9

Stereospecific CC-bond formation with rabbit muscle aldolase - A chemoenzymatic synthesis of (+)-exo-brevicomin

Michael K. Schultz, Herbert Waldmann, Walter Vogt et al. · Tetrahedron Letters · 1990 · 35 citations

, , +10