Organometallic reagents primed for peptide modification

Cecile Elgindy; Lara R. Malins

doi:10.1016/j.checat.2021.06.020

Organometallic reagents primed for peptide modification

Cecile Elgindy, Lara R. Malins^*

^*Corresponding author for this work

Research School of Chemistry

Research output: Contribution to journal › Comment/debate › peer-review

1 Citation (Scopus)

Abstract

In this issue of Chem Catalysis, Walczak and co-workers introduce a carbastannatrane alanine derivative that facilitates amino acid side-chain functionalizations via C–C, C–S, and C–Se bond formation using Stille cross-coupling reactions. Applications in late-stage peptide modifications and macrocyclizations further exemplify the value of this novel building block.

Original language	English
Pages (from-to)	758-760
Number of pages	3
Journal	Chem Catalysis
Volume	1
Issue number	4
DOIs	https://doi.org/10.1016/j.checat.2021.06.020
Publication status	Published - 16 Sept 2021

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10.1016/j.checat.2021.06.020

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title = "Organometallic reagents primed for peptide modification",

abstract = "In this issue of Chem Catalysis, Walczak and co-workers introduce a carbastannatrane alanine derivative that facilitates amino acid side-chain functionalizations via C–C, C–S, and C–Se bond formation using Stille cross-coupling reactions. Applications in late-stage peptide modifications and macrocyclizations further exemplify the value of this novel building block.",

author = "Cecile Elgindy and Malins, \{Lara R.\}",

note = "Publisher Copyright: {\textcopyright} 2021 Elsevier Inc.",

year = "2021",

month = sep,

day = "16",

doi = "10.1016/j.checat.2021.06.020",

language = "English",

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pages = "758--760",

journal = "Chem Catalysis",

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T1 - Organometallic reagents primed for peptide modification

AU - Elgindy, Cecile

AU - Malins, Lara R.

PY - 2021/9/16

Y1 - 2021/9/16

N2 - In this issue of Chem Catalysis, Walczak and co-workers introduce a carbastannatrane alanine derivative that facilitates amino acid side-chain functionalizations via C–C, C–S, and C–Se bond formation using Stille cross-coupling reactions. Applications in late-stage peptide modifications and macrocyclizations further exemplify the value of this novel building block.

AB - In this issue of Chem Catalysis, Walczak and co-workers introduce a carbastannatrane alanine derivative that facilitates amino acid side-chain functionalizations via C–C, C–S, and C–Se bond formation using Stille cross-coupling reactions. Applications in late-stage peptide modifications and macrocyclizations further exemplify the value of this novel building block.

UR - https://www.scopus.com/pages/publications/85126079376

U2 - 10.1016/j.checat.2021.06.020

DO - 10.1016/j.checat.2021.06.020

M3 - Comment/debate

AN - SCOPUS:85126079376

SN - 2667-1107

VL - 1

SP - 758

EP - 760

JO - Chem Catalysis

JF - Chem Catalysis

IS - 4

ER -

Organometallic reagents primed for peptide modification

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