67321-60-2Relevant academic research and scientific papers
STEREOCHEMISTRY OF THE METHYLATION OF THE (11S,4S) AND (11S,4R) DIASTEREOMERS OF 4-METHYL-1-(α-METHYLBENZYL)AZETIDIN-2-ONE
Romanova, N. N.,Tallo, T. G.,Borisenko, A. A.,Bundel', Yu. G.
, p. 761 - 766 (1990)
The methylation of the lithium derivatives of the (11S,4S) and (11S,4R) diastereomers of 4-methyl-1-(α-methylbenzyl)azetidin-2-one proceeds stereospecifically with the formation of only trans-(3S,4S)- and trans-(3R,4R)-dimethyl-1-(S
Synthesis and Stereochemistry of Chiral Azetidin-2-ones and Azetidine-2-thiones. I. Synthesis of Diastereomeric 2- and 3-Substituted N-(α-Methylbenzyl)-β-aminopropionic Acids
Romanova, N. N.,Tallo, T. G.,Bundel', Yu. G.
, p. 375 - 377 (2007/10/03)
Nucleophilic addition of α-methylbenzylamine to the double bond of 2- and 3-substituted acrylic acids in pyridine under reflux proceeds nonstereoselectively.
