(PDF) Designing Silylated L -Amino Acids Using a Wittig

Designing Silylated L -Amino Acids Using a Wittig Strategy: Synthesis of Peptide Derivatives and 18 F-Labelling

European Journal of Organic Chemistry - Germany

doi 10.1002/ejoc.201701170

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Date

September 29, 2017

Authors

Raluca Malacea-Kabbara

Publisher

Wiley

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Designing Silylated L -Amino Acids Using a Wittig Strategy: Synthesis of Peptide Derivatives and 18 F-Labelling

European Journal of Organic Chemistry - Germany

doi 10.1002/ejoc.201701170

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Hydantoin Derivatives of L- And D-Amino Acids: Synthesis and Evaluation of Their Antiviral and Antitumoral Activity

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Peptide‐Chain Elongation Using Unprotected Amino Acids in a Micro‐Flow Reactor

Peptide Synthesis in Water IV. Preparation of N-Ethanesulfonylethoxycarbonyl (Esc) Amino Acids and Their Application to Solid Phase Peptide Synthesis

Synthesis of Bicyclic Tertiary A-Amino Acids

Synthesis of Bicyclic Tertiary A-Amino Acids

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