The Wolff-Kishner reduction is a method used to reduce carbonyl compounds (aldehydes and ketones) to methylene groups (\(-{CH2}-\)) using hydrazine (\({NH2NH2}\)) and a strong base like potassium hydroxide (\({KOH}\)).
General Reaction:
\[ {R-CHO} \xrightarrow[{KOH}]{{NH2NH2}} {R-CH3} \]
This reaction effectively removes the oxygen of the carbonyl group and replaces it with two hydrogen atoms, converting aldehydes/ketones to alkanes.
The decarboxylation reaction involves the loss of a carbon dioxide molecule (\({CO2}\)) from a carboxylic acid, resulting in the formation of a corresponding hydrocarbon.
General Reaction:
\[ {R-COOH} \xrightarrow{\text{heat}} {R-H} + {CO2} \]
This reaction typically occurs upon heating and is often catalyzed by soda lime or mineral acids.
Match the Compounds (List - I) with the appropriate Catalyst/Reagents (List - II) for their reduction into corresponding amines. 
Consider the following amino acid: 
Which of the following options contain the correct structure of (A) and (B)?