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  Native chemical ligation in dimethylformamide can be performed chemoselectively without racemization

Dittmann, M., Sadek, M., Seidel, R., & Engelhard, M. (2012). Native chemical ligation in dimethylformamide can be performed chemoselectively without racemization. Journal of Peptide Science, 18(5): 1, pp. 312-316. Retrieved from http://dx.doi.org/10.1002/psc.2401.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0013-FF11-A Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0013-FF12-8
Genre: Journal Article

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 Creators:
Dittmann, Marc1, Author
Sadek, Muheeb1, Author
Seidel, Ralf2, Author           
Engelhard, Martin2, Author           
Affiliations:
1Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753286              
2Abt. III: Physikalische Biochemie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753289              

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Free keywords: native chemical ligation in organic solvents; peptide synthesis; hydrophobic peptides, racemization
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Language(s): eng - English
 Dates: 2012-03-19
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 609025
URI: http://dx.doi.org/10.1002/psc.2401
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Title: Journal of Peptide Science
Source Genre: Journal
 Creator(s):
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Publ. Info: -
Pages: - Volume / Issue: 18 (5) Sequence Number: 1 Start / End Page: 312 - 316 Identifier: -