6 research outputs found
rac-2,2′-Bipiperidine-1,1′-diium dibromide
In the title compound, C10H22N2
2+·2Br−, a precursor in the synthesis of organocatalysts, the bipiperidinium ion is located on a twofold rotation axis which passes through the mid-point of the central C—C bond. The piperidinium ring adopts a chair conformation. In the crystal, the cations are linked together by Br− ions through N—H⋯Br hydrogen bonds, forming layers parallel to the ab plane
Synthesis of Heterobicyclo[3.2.0]heptane Derivatives via Multicomponent Cascade Reaction. Heterobits\ufcklo[3.2.0]heptaanide s\ufcntees multikomponentse kaskaadreaktsiooniga
Synthesis of Heterobicyclo[3.2.0]heptane Derivatives via Multicomponent Cascade Reaction. Heterobits\ufcklo[3.2.0]heptaanide s\ufcntees multikomponentse kaskaadreaktsiooniga
Diastereoselective Multicomponent Cascade Reaction Leading to [3.2.0]-Heterobicyclic Compounds
A general three-component triple cascade reaction through
an iminium–enamine–iminium
sequential activation initiated by a hetero-Michael addition to α,β-unsaturated
aldehydes affords [3.2.0]heterobicycles in high diastereoselectivity.
The rate and diastereoselectivity of the reaction depended on the
(<i>E</i>)-4-heterocrotonate and size of the secondary amine.
The enantiomers of the major diastereoisomer of oxa- and azabicyclo[3.2.0]heptane
derivatives were separated by enzymatic kinetic resolution with immobilized <i>Candida antarctica</i> Lipase
B (CALB), with <i>E</i> values up to 153. The absolute configuration
of the nonacylated enantiomer of oxabicyclo[3.2.0]heptane was determined
by single crystal X-ray analysis
Diastereoselective Multicomponent Cascade Reaction Leading to [3.2.0]-Heterobicyclic Compounds
A general three-component triple cascade reaction through
an iminium–enamine–iminium
sequential activation initiated by a hetero-Michael addition to α,β-unsaturated
aldehydes affords [3.2.0]heterobicycles in high diastereoselectivity.
The rate and diastereoselectivity of the reaction depended on the
(<i>E</i>)-4-heterocrotonate and size of the secondary amine.
The enantiomers of the major diastereoisomer of oxa- and azabicyclo[3.2.0]heptane
derivatives were separated by enzymatic kinetic resolution with immobilized <i>Candida antarctica</i> Lipase
B (CALB), with <i>E</i> values up to 153. The absolute configuration
of the nonacylated enantiomer of oxabicyclo[3.2.0]heptane was determined
by single crystal X-ray analysis