Catalysts

(Z)-N′-Cyanopicolinimidamide.

(Z)-N′-Cyanopicolinimidamide.

Camphor quinone (CQ) can absorb UV radiation (due to π π * transition) and visible light in the range of 400-500nm (due to N, π * transition of α - dicarbonyl chromophore).

Camphor quinone (CQ) can absorb UV radiation (due to π π * transition) and visible light in the range of 400-500nm (due to N, π * transition of α - dicarbonyl chromophore).

Camphor quinone (CQ) can absorb UV radiation (due to π π * transition) and visible light in the range of 400-500nm (due to N, π * transition of α - dicarbonyl chromophore).

Camphor quinone (CQ) can absorb UV radiation (due to π π * transition) and visible light in the range of 400-500nm (due to N, π * transition of α - dicarbonyl chromophore).

DescriptionDuPhos and BPE Ligands: Highly Efficient Privileged Ligands(−)-1,2-Bis((2R,5R)-2,5-diphenylphospholano)ethane can be used:As a chiral ligand in the 1,3-dipolar cycloaddition reaction of azomethyne yielded [70]fullerene enantiomers:

DescriptionDuPhos and BPE Ligands: Highly Efficient Privileged Ligands(−)-1,2-Bis((2R,5R)-2,5-diphenylphospholano)ethane can be used:As a chiral ligand in the 1,3-dipolar cycloaddition reaction of azomethyne yielded [70]fullerene enantiomers:

DescriptionDuPhos and BPE Ligands: Highly Efficient Privileged Ligands(−)-1,2-Bis((2R,5R)-2,5-diphenylphospholano)ethane can be used:As a chiral ligand in the 1,3-dipolar cycloaddition reaction of azomethyne yielded [70]fullerene enantiomers:

(−)-1,4-Bis-O-(4-chlorobenzyl)-L-threitol.

Description(-)-1-(9-Fluorenyl)ethyl chloroformate is mostly used as an in-capillary derivatization agent for the separation of amino acid (AA) derivatives by micellar electrokinetic chromatography (MEKC).

(−)-3-(Trifluoroacetyl)camphor.