Synthesis of methyl pyropheophorbide-d derivatives possessing the 3-acyl groups and their electronic absorption spectra
書誌事項
- 公開日
- 2016-06
- 資源種別
- journal article
- 権利情報
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- https://www.elsevier.com/tdm/userlicense/1.0/
- DOI
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- 10.1016/j.tet.2016.04.074
- 公開者
- Elsevier BV
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説明
Abstract Methyl 3-acyl-pyropheophorbides-a were prepared by modification of naturally occurring chlorophyll-a through Grignard or Barbier reactions of the 3-formyl group and successive Ley–Griffith or Dess–Martin oxidations of the resulting secondary alcohols. The semi-synthetic 3-acyl-chlorins gave intense visible bands in dichloromethane and the absorption spectra were dependent on the 31-substituents. The larger π-conjugation of the 3-acyl group with the chlorin moiety shifted the visible absorption maxima to longer wavelengths.
収録刊行物
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- Tetrahedron
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Tetrahedron 72 (24), 3477-3489, 2016-06
Elsevier BV
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詳細情報 詳細情報について
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- CRID
- 1360004232525377280
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- ISSN
- 00404020
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- 資料種別
- journal article
-
- データソース種別
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- Crossref
- KAKEN
- OpenAIRE
- IRDB

