An article Regio- and Chemoselective Deprotection of Primary Acetates by Zirconium Hydrides WOS:000464247500003 published article about IN-SITU GENERATION; ALKYLALUMINUM HYDRIDE; TERTIARY AMIDES; ONE-POT; REDUCTION; DEACETYLATION; CP2ZR(H)CL; ALDEHYDES; HYDROZIRCONATION; CYCLODEXTRINS in [Gavel, Marine; Courant, Thibaut; Joosten, Antoine Yvan Philippe; Lecourt, Thomas] Normandie Univ, INSA Rouen, CNRS, UMR 6014,COBRA,UNIROUEN, F-76000 Rouen, France in 2019, Cited 47. The Name is 4-Methoxybenzyl acetate. Through research, I have a further understanding and discovery of 104-21-2. Recommanded Product: 4-Methoxybenzyl acetate
A combination of DIBAL-H and Cp2ZrCl2 is shown to promote the regioselective cleavage of primary acetates on a broad scope of substrates, ranging from carbohydrates to terpene derivatives, with a high tolerance toward protecting groups and numerous functionalities found in natural products and bioactive compounds. Apart from providing highly valuable building blocks in only two steps from biosourced raw materials, this selective de-O-acetylation should also be strongly helpful to solve selectivity issues in organic synthesis.
Recommanded Product: 4-Methoxybenzyl acetate. Welcome to talk about 104-21-2, If you have any questions, you can contact Gavel, M; Courant, T; Joosten, AYP; Lecourt, T or send Email.
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem