4.7 Article

Total Syntheses of the Proposed Biosynthetic Intermediates of Tetrodotoxin Tb-210B, Tb-226, Tb-242C, and Tb-258

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 87, Issue 14, Pages 9023-9033

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.2c00704

Keywords

-

Funding

  1. Frontier Research on Chemical Communication [17H06406]
  2. Middle Molecular Strategy ? [18H04400]
  3. MEXT
  4. MEXT [17H06406, 18H04400, 19H02896]
  5. Nagoya University

Ask authors/readers for more resources

The collective synthesis of four spiro-cyclic guanidines isolated from puffer fish, which are considered possible biosynthetic intermediates of tetrodotoxin, has been achieved through stepwise deoxygenation or hydroxylation of a common intermediate.
The collective synthesis of the four spiro-cyclic guanidines Tb-210B, Tb-226, Tb-242C, and Tb-258, all of which have been isolated from puffer fish and are considered possible biosynthetic intermediates of tetrodotoxin, has been achieved. Our synthesis is based on the stepwise deoxygenation or hydroxylation of a common intermediate, prepared from a known oxazoline.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available