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Heterospirocyclic 3-Amino-2H-azirines as Convenient Building Blocks in Peptide Synthesis

Date

Date

Date
2019
Journal Article
Published version

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Strässler, C., & Heimgartner, H. (2019). Heterospirocyclic 3-Amino-2H-azirines as Convenient Building Blocks in Peptide Synthesis. Heterocycles, 99(1), 446. https://doi.org/10.3987/COM-18-S(F)41

Abstract

Abstract

Abstract

Heterospirocyclic 3-amino-2H-azirines with a tetrahydropyran (Thp), tetrahydrothiopyran (Tht), or N-protected piperidine (Pip) moiety are useful reagents for the preparation of peptides containing the corresponding six-membered heterocyclic 4-amino-4-carboxylic acid unit. In the present study, tripeptides of the type H-Asp-D-Ala-Xaa-OMe, where Xaa is the heterocyclic amino acid, were prepared according to the ‘azirine/oxazolone method’.

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Creators (Authors)

  • Strässler, Christoph
    affiliation.icon.alt
  • Heimgartner, Heinz
    affiliation.icon.alt

Journal/Series Title

Journal/Series Title

Journal/Series Title

Volume

Volume

Volume
99

Number

Number

Number
1

Page Range

Page Range

Page Range
446

Item Type

Item Type

Item Type
Journal Article

Dewey Decimal Classifikation

Dewey Decimal Classifikation

Dewey Decimal Classifikation

Language

Language

Language
English

Publication date

Publication date

Publication date
2019-01-01

Date available

Date available

Date available
2018-10-31

Publisher

Publisher

Publisher

ISSN or e-ISSN

ISSN or e-ISSN

ISSN or e-ISSN
0385-5414

OA Status

OA Status

OA Status
Green

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Citation copied

Strässler, C., & Heimgartner, H. (2019). Heterospirocyclic 3-Amino-2H-azirines as Convenient Building Blocks in Peptide Synthesis. Heterocycles, 99(1), 446. https://doi.org/10.3987/COM-18-S(F)41

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