Photochemically induced symmetrical coupling reactions between cyclohexa-2,4-dienones and alpha,omega-diamines. A new approach to the selective labelling of peptides and proteins
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- Title
- Photochemically induced symmetrical coupling reactions between cyclohexa-2,4-dienones and alpha,omega-diamines. A new approach to the selective labelling of peptides and proteins
- Authors
- Barton, DHR; Chung, SK; Kim, YM; Kwon, TW
- Date Issued
- 1997-03-18
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Abstract
- 2,4,6-Trimethylcyclohexa-2,4-dien-1-one derivatives undergo ring cleavage to furnish symmetrical amides on irradiation with visible light in the presence of various alpha,omega-diamines. Five different symmetrical amides containing a substituted diene moiety were synthesized in 65-85% yield. (C) 1997 Elsevier Science Ltd.
- URI
- https://oasis.postech.ac.kr/handle/2014.oak/21360
- DOI
- 10.1016/S0960-894X(97)00096-6
- ISSN
- 0960-894X
- Article Type
- Article
- Citation
- BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 7, no. 6, page. 733 - 738, 1997-03-18
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