An article The Detosylation of Chiral 1,2-Bis(tosylamides) WOS:000670661000054 published article about INNER-SPHERE PROCESSES; OUTER-SPHERE; QUANTITATIVE-EVALUATION; SULFONYL GROUP; DEPROTECTION; MAGNESIUM; REDUCTION; CLEAVAGE; ELEMENTS; LITHIUM in [Gaston, Jayden J.; Tague, Andrew J.; Smyth, Jamie E.; Butler, Nicholas M.; Yu, Haibo; Keller, Paul A.] Univ Wollongong, Sch Chem & Mol Biosci, Mol Horizons, Wollongong, NSW 2522, Australia; [Gaston, Jayden J.; Tague, Andrew J.; Smyth, Jamie E.; Butler, Nicholas M.; Yu, Haibo; Keller, Paul A.] Illawarra Hlth & Med Res Inst, Wollongong, NSW 2522, Australia; [Willis, Anthony C.] Australian Natl Univ, Sch Chem, Canberra, ACT 2601, Australia; [Hommes, Nico van Eikema; Clark, Timothy] Friedrich Alexander Univ Erlangen Nurnberg, Comp Chem Ctr, Dept Chem & Pharm, D-91052 Erlangen, Germany in 2021, Cited 52. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Formula: C8H10O2
The deprotection of chiral 1,2-bis(tosylamides) to their corresponding 1,2-diamines is mostly unsuccessful under standard conditions. In a new methodology, the use of Mg/MeOH with sufficient steric additions allows the facile synthesis of 1,2-diamines in 78-98% yields. These results are rationalized using density functional theory and the examination of inner and outer-sphere reduction mechanisms.
Formula: C8H10O2. Bye, fridends, I hope you can learn more about C8H10O2, If you have any questions, you can browse other blog as well. See you lster.
Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts