290838-42-5Relevant articles and documents
Desymmetrization of aziridine with malononitrile using cinchona alkaloid amide/zinc(ii) catalysts
Shiomi, Noriyuki,Kuroda, Mami,Nakamura, Shuichi
, p. 1817 - 1820 (2017)
The catalytic enantioselective desymmetrization of aziridines with malononitrile has been developed. Good yield and enantioselectivity were obtained by using cinchona alkaloid amide/Zn(ii) catalysts. The obtained product can be converted to β-aminoester,
Synthesis of Cyclic β-Amino Acid Esters from Methionine, Allylglycine, and Serine
Gardiner, James,Anderson, Kelly H.,Downard, Alison,Abell, Andrew D.
, p. 3375 - 3382 (2007/10/03)
Here we report a versatile ring-closing metathesis-based approach to 5-, 6-, and 7-membered cyclic β-amino esters starting with simple and readily available building blocks-methionine, allylglycine, and serine-where the nature of the amino acid determines
(R,R,R)-2,5-diaminocylohexanecarboxylic acid, a building block for water-soluble, helix-forming β-peptides
Appella, Daniel H.,LePlae, Paul R.,Raguse, Tami L.,Gellman, Samuel H.
, p. 4766 - 4769 (2007/10/03)
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