Mukherjee, Sumit published the artcileApplication of Tandem Ring-Closing Enyne Metathesis: Formal Total Synthesis of (-)-Cochleamycin A, Application of (+)-B-Methoxydiisopinocampheylborane, the publication is Organic Letters (2009), 11(13), 2916-2919, database is CAplus and MEDLINE.
A tandem ring-closing metathesis of a silaketal-based dienyne substrate proceeded efficiently to provide a bicyclic siloxane, which upon removal of the silicon tether afforded an (E,Z)-1,3-dienediol. Further manipulation of this key functional motif rendered synthesis of the entire C1-C19 linear skeleton of (-)-cochleamycin A (I) , a late-stage intermediate employed in the previous total synthesis of (+)-cochleamycin A by Roush and co-workers.
Organic Letters 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 C21H37BO, Application of (+)-B-Methoxydiisopinocampheylborane.
Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem