Garnes-Portoles, Francisco; Miguelez, Ruben; Grayson, Matthew N.; Barrio, Pablo published an article in 2022. The article was titled 《Heteroatom-Tethered ω-Alkenylallylboronates: Stereoselective Synthesis of Heterocyclic Derived Alcohols》, and you may find the article in Synthesis.Reference of 2-(Benzyloxy)acetaldehyde The information in the text is summarized as follows:
The synthesis of ω-alkenylallylboronates using a heteroatom tether to join both functional groups was described for the first time. Then, these unprecedented compounds were used in a tandem Bronsted acid catalyzed allylboration/ring-closing metathesis (RCM) reaction affording heterocyclic derived alcs. as single diastereoisomers. The low enantioselectivity observed in the asym. version using a chiral phosphoric acid catalyst was studied theor. The results came from multiple reactions, including the reaction of 2-(Benzyloxy)acetaldehyde(cas: 60656-87-3Reference of 2-(Benzyloxy)acetaldehyde)
2-(Benzyloxy)acetaldehyde(cas: 60656-87-3) may be used in the following syntheses: (3S,5S)-methyl 6-benzyloxy-3,5-dihydroxyhexanoate ,(S)-5-benzyloxy-4-hydroxypentan-2-one, myxothiazols.Reference of 2-(Benzyloxy)acetaldehyde
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem