Wang, Xiang published the artcileTotal Synthesis of the Salicylate Enamide Macrolide Oximidine II, Synthetic Route of 99438-28-5, the publication is Journal of the American Chemical Society (2003), 125(20), 6040-6041, database is CAplus and MEDLINE.
The asym. synthesis of the salicylate enamide macrolide oximidine II (I) is reported. The synthesis involves a highly regio- and stereoselective ring-closing metathesis of a bis-diene substrate to construct the macrocyclic triene core. Copper(I)-mediated amidation of a (Z)-vinyl iodide was employed to attach the enamide side chain.
Journal of the American Chemical Society published new progress about 99438-28-5. 99438-28-5 belongs to ethers-buliding-blocks, auxiliary class Chiral,Aliphatic cyclic hydrocarbon, name is (+)-B-Methoxydiisopinocampheylborane, and the molecular formula is C5H5F3O2, Synthetic Route of 99438-28-5.
Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem