Synthesis of Silacyclic Dipeptides: Peptide Elongation at Both N- and C-Termini of Dipeptide
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- Tomohiro Hattori
- Peptide Research Center, Chubu University, 1200 Matsumoto-cho, Kasugai, Aichi 487-8501, Japan
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- Hisashi Yamamoto
- Peptide Research Center, Chubu University, 1200 Matsumoto-cho, Kasugai, Aichi 487-8501, Japan
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説明
A new type of peptide bond formation utilizing silacyclic amino acids or peptides is described. This work has the following advantages: (1) imidazolylsilane is a highly fascinating coupling reagent for dipeptide synthesis from N-,C-terminal unprotected amino acids with amino acid
収録刊行物
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- Journal of the American Chemical Society
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Journal of the American Chemical Society 144 (4), 1758-1765, 2022-01-21
American Chemical Society (ACS)
関連研究データ
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キーワード
- Chemical Sciences not elsewhere classified
- Physiology
- Nitrogen
- Biophysics
- silacyclic compounds
- pot site
- innovative advantages
- Biochemistry
- Microbiology
- Peptides, Cyclic
- c ‑ termini
- cyclized products show
- selective tetra
- reaction conditions
- new type
- Virology
- >- butyl esters
- Molecular Biology
- oligopeptide syntheses
- Evolutionary Biology
- capacity lead
- Dipeptides
- >- butyl ester
- Silanes
- 540
- tert </
- Carbon
- c
- Cyclization
- n -
- peptide elongation
- Medicine
- remarkable capacity
- following advantages
- silacyclic dipeptides
- amino acid
- Developmental Biology
詳細情報 詳細情報について
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- CRID
- 1360576118694987392
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- ISSN
- 15205126
- 00027863
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- PubMed
- 35060715
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- 資料種別
- journal article
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- データソース種別
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- Crossref
- KAKEN
- OpenAIRE
