A highly regioselective Lewis acid-mediated SN2-type ring-opening of N-sulfonylaziridines
and azetidines with tetraalkylammonium halides in CH2Cl2 solution to afford 1, 2-and 1, 3 …

Introduction β-Amino acids might be regarded as the building blocks that nature overlooked.
Although seldom used in nature, scientists have recognized the importance of β-amino acids …

Direct amination of unactivated allylic alcohols with aqueous ammonia was catalyzed by a
Pt/phosphine complex to give the corresponding allylamines along with water as the sole by …

The palladium-catalyzed, substrate-directable Heck–Matsuda reaction of allylamine
derivatives with arenediazonium salts is reported. The reaction proceeds under mild …

Herein, a photoinduced, Pd-catalyzed direct 1, 2-carboamination of conjugated 1, 3-dienes
has been successfully achieved. Sequential regioselective C–C bond and enantioselective …

An asymmetric Mannich reaction of silyl ketene acetals with N-Boc-amino sulfones has been
developed. A chiral disulfonimide efficiently catalyzes both the in situ generation of the …

Einfach gut: Die durch das Chinidinamid 1 katalysierte [2+ 2]‐Cycloaddition von N‐
Sulfonyliminen 2 und Alkyl‐2, 3‐butadienoaten 3 lieferte die R‐konfigurierten Azetidine 4 in …

Lewis acid catalyzed quaternary ammonium salt mediated highly regioselective ring-
opening of chiral activated aziridines and azetidines with alcohols to nonracemic β-and γ …

A highly enantio-and diastereoselective Lewis acid catalyzed SN2-type ring opening
followed by cyclization of aziridines with active methylene carbon nucleophiles to …

A highly regio-and stereoselective strategy for the syntheses in high yield and
enantioselectivity of a variety of substituted nonracemic morpholines and their homologues …