Sorption and Separation of Optical Isomers of 2-Butanol by Chiral Porous Coordination Polymers

Theoretical and Experimental Chemistry - It was shown that porous coordination polymers (PCPs) of 3d metals containing chiral centers in fragments of deprotonated (S)-lactic and (R)-aspartic acid...     

Synthesis of 2‐Unsubstituted 1,3‐Selenazoles by Cyclization of Selenoformamide with α‐Bromocarbonyl Compounds

2‐Unsubstituted 1,3‐selenazoles were prepared by cyclization of selenoformamide with α‐bromoacetophenones. Parent 1,3‐selenazole was prepared by cyclization of selenoformamide with α‐bromoacetaldehyde.     

Formation of Heterocyclic and Polycyclic Compounds from Amino Alcohols and Dialdehydes

Amino alcohols typically react with aldehydes to produce oxazolidines. It was hypothesized that the condensation of several commercially available amino alcohols with dialdehydes would produce a series of bicyclic oxazolidines containing two secondary amines. However, there were remarkable differences in the type of products formed depending on the structure of the dicarbonyl compounds and the reaction conditions. When linear aliphatic dialdehydes such as glyoxal were used, the expected bis‐oxazolidines were not produced; instead, polycyclic structures or oxazines were formed. However, when cyclic dialdehydes such as 1,3/1,4 cyclohexane dicarboxaldehyde were used, they resulted in products bearing the desired oxazolidine moieties.     

Structure of 3,3:6,6-dibutano-3a-methyl-6a-phenyltetrahydrofuro[3,2-b]furan-2,5-dione

Journal of Structural Chemistry - In the interaction of methyl 1-bromocyclopentanecarboxylate with zinc and 1-phenylpropan-1,2-dione,...