Published June 2, 2017 | Version Supplemental Material + Accepted Version
Journal Article Open

Improved Synthesis for Modular Ascarosides Uncovers Biological Activity

  • 1. ROR icon Cornell University
  • 2. ROR icon California Institute of Technology
  • 3. ROR icon Worcester Polytechnic Institute

Abstract

A versatile synthesis of modular ascarosides, a family of signaling molecules from Caenorhabditis elegans and other nematodes, via hydrogenolysis of a cyclic sulfate derived from methyl-α-l-rhamnopyranoside is reported. The route enables selective introduction of different side chains at the 1, 2, and 4 positions of the sugar, as demonstrated for ascarosides from C. elegans and Pristionchus pacificus. Bioassays with synthetic samples of 4′-tigloyl ascaroside mbas#3 revealed its role as an avoidance or dispersal signal.

Additional Information

© 2017 American Chemical Society. Received: April 3, 2017; Published: May 17, 2017. This work was supported in part by the NIH (GM113692 and GM088290 to FCS) and the Howard Hughes Medical Institute. We thank Robert J. Micikas (University of Pennsylvania) for helpful comments and Alexander Artyukhin (Boyce Thompson Institute) for assistance with mass spectrometry.

Attached Files

Accepted Version - nihms877819.pdf

Supplemental Material - ol7b01009_si_001.pdf

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Additional details

Identifiers

PMCID
PMC5533076
Eprint ID
77564
DOI
10.1021/acs.orglett.7b01009
Resolver ID
CaltechAUTHORS:20170518-101558193

Funding

NIH
GM113692
NIH
GM088290
Howard Hughes Medical Institute (HHMI)

Dates

Created
2017-05-18
Created from EPrint's datestamp field
Updated
2022-03-28
Created from EPrint's last_modified field