Little discovery in the laboratory: a new route for 4221-99-2

When you point to this article, it is believed that you are also very interested in this compound(4221-99-2)Application In Synthesis of (S)-Butan-2-ol and due to space limitations, I can only present the most important information.

Application In Synthesis of (S)-Butan-2-ol. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: (S)-Butan-2-ol, is researched, Molecular C4H10O, CAS is 4221-99-2, about Straightforward N-alkylation of diketopyrrolopyrroles through the Mitsunobu reaction with benzyl, α-branched, and chiral alcohols. Author is Mastropasqua Talamo, Maurizio; Pop, Flavia; Avarvari, Narcis.

The N-alkylation of diketopyrrolopyrroles (DPPs) I (Ar = 2-thienyl, 4-bromophenyl, 2-pyridyl) represents a fundamental step to ensure solubility and further processability. Commonly used nucleophilic substitution in halogenated derivatives is replaced in this work by the Mitsunobu reaction affording unprecedented DPPs with α-branched and chiral chains e.g., II.

When you point to this article, it is believed that you are also very interested in this compound(4221-99-2)Application In Synthesis of (S)-Butan-2-ol and due to space limitations, I can only present the most important information.

Reference:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem