The effect of the change of 538-58-9 synthetic route on the product

This molecular description is the mechanism of the reaction; it describes how individual atoms, ions, or molecules interact to form particular products.If you are interested, you can also browse other articles of 1,5-Diphenylpenta-1,4-dien-3-one, We look forward to the emergence of more reaction modes in the future.

538-58-9, An elementary termolecular reaction involves the simultaneous collision of three atoms, molecules, or ions.24621-61-2, name is (S)-Butane-1,3-diol. Here is a downstream synthesis route of the compound 24621-61-2

General procedure: General procedure (GP): Dienones 2a-m (0.25 mmol) and diamide 1a or 1b (74 mg, 0.25 mmol)were dissolved in 10 mL of dry CH2Cl2 in a 25 mL round bottom flask. DBU (3 eq, 114 mg, 0.75 mmol)was added to the reaction, which was subsequently stirred for 2-3 h. After the reaction was completedas determined by TLC, the crude material was subjected to column chromatography using ethylacetate/n-hexane (2:3) to give the desired compounds 3a-m.

This molecular description is the mechanism of the reaction; it describes how individual atoms, ions, or molecules interact to form particular products.If you are interested, you can also browse other articles of 1,5-Diphenylpenta-1,4-dien-3-one, We look forward to the emergence of more reaction modes in the future.

Reference£º
Article; Al-Majid, Abdullah Mohammed; Islam, Mohammad Shahidul; Atef, Saleh; El-Senduny, Fardous F.; Badria, Farid A.; Elshaier, Yaseen A. M. M.; Ali; Barakat, Assem; Motiur Rahman; Molecules; vol. 24; 7; (2019);,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate