70546-93-9Relevant academic research and scientific papers
Direct catalytic synthesis of unprotected 2-amino-1-phenylethanols from alkenes by using iron(II) phthalocyanine
Legnani, Luca,Morandi, Bill
, p. 2248 - 2251 (2016)
Aryl-substituted amino alcohols are privileged scaffolds in medicinal chemistry and natural products. Herein, we report that an exceptionally simple and inexpensive FeII complex efficiently catalyzes the direct transformation of simple alkenes into unprotected amino alcohols in good yield and perfect regioselectivity. This new catalytic method was applied in the expedient synthesis of bioactive molecules and could be extended to aminoetherification.
Shahidine, a novel and highly labile oxazoline from Aegle marmelos: the parent compound of aegeline and related amides
Faizi, Shaheen,Farooqi, Fatima,Zikr-Ur-Rehman, Sadia,Naz, Aneela,Noor, Fatima,Ansari, Farheen,Ahmad, Aqeel,Khan, Shakeel Ahmed
body text, p. 998 - 1004 (2009/05/09)
A rare alkaloid, shahidine (1), having an unstable oxazoline core has been isolated as a major constituent from the fresh leaves of Aegle marmelos. It is moisture-sensitive, and found to be the parent compound of aegeline and other amides, however, it is
