Literature DB >> 8244630

Allyl-based groups for side-chain protection of amino-acids.

A Loffet, H X Zhang.   

Abstract

Allyl and allyloxycarbonyl groups are used for the side-chain protection of amino acids. The protecting groups may be selectively cleaved using the reagent HSnBu3 under palladium catalysis. The preparation of Boc and Fmoc series of protected amino acids is described.

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Year:  1993        PMID: 8244630     DOI: 10.1111/j.1399-3011.1993.tb00504.x

Source DB:  PubMed          Journal:  Int J Pept Protein Res        ISSN: 0367-8377


  4 in total

1.  Encoded combinatorial chemistry: synthesis and screening of a library of highly functionalized pyrrolidines.

Authors:  D Maclean; J R Schullek; M M Murphy; Z J Ni; E M Gordon; M A Gallop
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-01       Impact factor: 11.205

2.  Strategies for the synthesis of labeled peptides.

Authors:  L Bibbs; N P Ambulos; S A Kates; A Khatri; K F Medzihradszky; G Osapay; S T Weintraub
Journal:  J Biomol Tech       Date:  2000-12

3.  Aspartate-modified doxorubicin on its N-terminal increases drug accumulation in LAT1-overexpressing tumors.

Authors:  Weidang Wu; Yan Dong; Jing Gao; Min Gong; Xing Zhang; Weiling Kong; Yazhuo Li; Yong Zeng; Duanyun Si; Zihong Wei; Xiaoyan Ci; Lixin Jiang; Wei Li; Quansheng Li; Xiulin Yi; Changxiao Liu
Journal:  Cancer Sci       Date:  2015-05-26       Impact factor: 6.716

Review 4.  Automated solid-phase peptide synthesis to obtain therapeutic peptides.

Authors:  Veronika Mäde; Sylvia Els-Heindl; Annette G Beck-Sickinger
Journal:  Beilstein J Org Chem       Date:  2014-05-22       Impact factor: 2.883

  4 in total

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