Conversion of 5-deoxypulchelloside I to caudatoside A.

  title={Conversion of 5-deoxypulchelloside I to caudatoside A.},
  author={Sloan Ayers and Albert T. Sneden},
  journal={Journal of natural products},
  volume={67 2},
The iridoid caudatoside A (2) was synthesized in seven steps from the naturally occurring iridoid 5-deoxypulchelloside I (1) using a straightforward series of protection and deprotection procedures to introduce the requisite C-6 cinnamoyl ester. 
3 Citations
1,3-Dioxins, Oxathiins, Dithiins, and their Benzo Derivatives
After introducing the subject, the application of theoretical methods for studying the NMR parameters (δ(1H, 13C), 1J(C, H), 3J(H, H)), both the rotational barrier of attached substituents and the
1,2-Dioxins, Oxathiins, Dithiins and Their Benzo Derivatives