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23 - PEPTIDES

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Total cards: 14•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (14)

#1
Front (Question)

what are the obstacles to RNA therapeutics

Back (Answer)

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#2
Front (Question)

what is the orientation and stereocemistry of amino acids

Back (Answer)

all have an L configuration all S except cysteine

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#3
Front (Question)

pKa of the amino and carboxyl groups of amino acids

Back (Answer)

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#4
Front (Question)

what AAs are the main constituents of collagen

Back (Answer)

glycine proline and hydroxyproline hydroxyproline is made by in vivo oxidation of proline, which requires vitamin C

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#5
Front (Question)

how is an aldol reaction catalysed by proline?

Back (Answer)

2021 nobel prise in chemistry

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#6
Front (Question)

what groups need to be protected so that condensation of peptide synthesis happens as desired

Back (Answer)

one AA: carboxy activated amino protected other AA: carboxy protected

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#7
Front (Question)

what are protecting groups for carboxylic acids

Back (Answer)

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#8
Front (Question)

what are protecting groups for amines

Back (Answer)

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#9
Front (Question)

how is fluorenemethyloxycarbonyl (Fmoc) removed?

Back (Answer)

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#10
Front (Question)

what is the tert-butoxycarbonyl (t-Boc) group and how is it removed?

Back (Answer)

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#11
Front (Question)

how does solid phase synthesis of a peptide happen?

Back (Answer)

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#12
Front (Question)

mechanism of DCC reaction

Back (Answer)

condensing reagent required for the reaction

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#13
Front (Question)

solid phase synthesis of nucleic acids, proteins and oligosaccharides and what needs to be controlled

Back (Answer)

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#14
Front (Question)

what is the general strategy for the solid phase synthesis of oligosaccharides

Back (Answer)

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