4.8 Article

Stereocontrolled Total Synthesis of Fucoxanthin and Its Polyene Chain-Modified Derivative

期刊

ORGANIC LETTERS
卷 14, 期 3, 页码 808-811

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ol203344c

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资金

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan [22550160]
  2. Matching Fund Subsidy for a Private University
  3. Grants-in-Aid for Scientific Research [24106741, 22550160, 10J07627] Funding Source: KAKEN

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Fucoxanthin exhibits high energy transfer efficiencies to Chlorophyll a (Chl a) in photosynthesis in the sea. In order to reveal how each characteristic functional group, such as the length of the polyene chain, allene, and conjugated carbonyl groups, of this marine natural product are responsible for its remarkably efficient ability, the total synthesis of fucoxanthin by controlling the stereochemistry was achieved. The method established for fucoxanthin synthesis was successfully applied to the synthesis of the C42 longer chain analogue.

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