Carbon-carbon bond forming reactions are simple and direct methods for synthesizing the
various skeletons and the diverse structures of organic compounds. Even 100 years after the …

A series of chiral (3R, 5R)-dihydroxypiperidine derivatives were conveniently prepared from
trans-4-hydroxy-l-proline and applied to the catalytic enantioselective addition of diethylzinc …

The realization of enantioselective CC-bond forming reactions is of immense importance in
the modern organic synthesis. The global needs of pharmaceutical industry and the fast …

The asymmetric addition of diethylzinc to aromatic and aliphatic aldehydes, including linear
aliphatic ones, catalyzed by 2mol% of β-amino alcohol (1S, 2R)-7, 7-dimethyl-1-morpholin-4 …

Carbohydrate‐based benzylidene acetals undergo reductive ring opening. 1‐β‐O‐Acyl
glucoside conjugates of phenylacetic acids have been synthesized, and their acyl migration …

Enantiopure norbornane-based γ-amino alcohols 1–4 have been obtained from (+)-
camphor and their catalytic behaviour as chiral ligands for the enantioselective addition of …

Valuable chiral sources of C (10)-substituted camphors and C (10)-substituted fenchones
can be straightforwardly obtained by treatment of an appropriate, easily obtainable, camphor …

Both cis-and trans-1, 2-amino alcohols 5 and their N-alkylated derivatives 6 were prepared
from (−)-α-pinene 7 as chirality source and utilized in asymmetric borane reduction of …

Methylidene substituted camphor was easily epoxidized to give bridgehead oxirane-
substituted camphor in the form of two diastereoisomers, isolated in pure form. These were …

Series of functionalized organolithium compounds were prepared and added to chiral
bicyclic ketones (1R-(+)-camphor analogue 2 and 1R-(−)-fenchone 3), resulting in the …