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Columbia University

Studies towards Selective Synthesis of Resveratrol-based Oligomeric Natural Products

Abstract

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๐˜Š๐˜ฉ๐˜ข๐˜ฑ๐˜ต๐˜ฆ๐˜ณ 1. ๐˜™๐˜ฆ๐˜ค๐˜ฆ๐˜ฏ๐˜ต ๐˜ด๐˜บ๐˜ฏ๐˜ต๐˜ฉ๐˜ฆ๐˜ต๐˜ช๐˜ค ๐˜ข๐˜ฑ๐˜ฑ๐˜ณ๐˜ฐ๐˜ข๐˜ค๐˜ฉ๐˜ฆ๐˜ด ๐˜ต๐˜ฐ๐˜ธ๐˜ข๐˜ณ๐˜ฅ๐˜ด ๐˜ต๐˜ฉ๐˜ฆ ๐˜ณ๐˜ฆ๐˜ด๐˜ท๐˜ฆ๐˜ณ๐˜ข๐˜ต๐˜ณ๐˜ฐ๐˜ญ ๐˜ง๐˜ข๐˜ฎ๐˜ช๐˜ญ๐˜บ ๐˜ฐ๐˜ง ๐˜ฐ๐˜ญ๐˜ช๐˜จ๐˜ฐ๐˜ฎ๐˜ฆ๐˜ณ๐˜ช๐˜ค ๐˜ฏ๐˜ข๐˜ต๐˜ถ๐˜ณ๐˜ข๐˜ญ ๐˜ฑ๐˜ณ๐˜ฐ๐˜ฅ๐˜ถ๐˜ค๐˜ต๐˜ด. This chapter outlines some of the past and present efforts in the field of resveratrol-based oligomeric natural product synthesis. Both biosynthetic approaches and stepwise synthetic approaches are discussed to present the current level of understanding regarding the controlled synthesis of these molecules in order to place the studies described in chapter 2 and 3 in better context. ๐˜Š๐˜ฉ๐˜ข๐˜ฑ๐˜ต๐˜ฆ๐˜ณ 2. ๐˜‹๐˜ฆ๐˜ท๐˜ฆ๐˜ญ๐˜ฐ๐˜ฑ๐˜ฎ๐˜ฆ๐˜ฏ๐˜ต ๐˜ฐ๐˜ง ๐˜ข ๐˜จ๐˜ฆ๐˜ฏ๐˜ฆ๐˜ณ๐˜ข๐˜ญ ๐˜ด๐˜บ๐˜ฏ๐˜ต๐˜ฉ๐˜ฆ๐˜ต๐˜ช๐˜ค ๐˜ฎ๐˜ฆ๐˜ต๐˜ฉ๐˜ฐ๐˜ฅ ๐˜ต๐˜ฐ๐˜ธ๐˜ข๐˜ณ๐˜ฅ๐˜ด ๐˜ฅ๐˜ช๐˜ง๐˜ง๐˜ฆ๐˜ณ๐˜ฆ๐˜ฏ๐˜ต ๐˜ฅ๐˜ช๐˜ฎ๐˜ฆ๐˜ณ๐˜ช๐˜ค ๐˜ด๐˜ต๐˜ณ๐˜ถ๐˜ค๐˜ต๐˜ถ๐˜ณ๐˜ฆ๐˜ด ๐˜ฐ๐˜ง ๐˜ต๐˜ฉ๐˜ฆ ๐˜ณ๐˜ฆ๐˜ด๐˜ท๐˜ฆ๐˜ณ๐˜ข๐˜ต๐˜ณ๐˜ฐ๐˜ญ ๐˜ง๐˜ข๐˜ฎ๐˜ช๐˜ญ๐˜บ. We have developed a general approach to achieve selective synthesis of the major dimeric architectures within the resveratrol family with the use of a unique key common intermediate possessing three aryl rings. Syntheses of three subclasses of resveratrol dimeric structures are reported. ๐˜Š๐˜ฉ๐˜ข๐˜ฑ๐˜ต๐˜ฆ๐˜ณ 3. ๐˜š๐˜บ๐˜ฏ๐˜ต๐˜ฉ๐˜ฆ๐˜ต๐˜ช๐˜ค ๐˜ฆ๐˜ง๐˜ง๐˜ฐ๐˜ณ๐˜ต๐˜ด ๐˜ต๐˜ฐ๐˜ธ๐˜ข๐˜ณ๐˜ฅ๐˜ด ๐˜ฅ๐˜ช๐˜ฉ๐˜บ๐˜ฅ๐˜ณ๐˜ฐ๐˜ฃ๐˜ฆ๐˜ฏ๐˜ป๐˜ฐ๐˜ง๐˜ถ๐˜ณ๐˜ข๐˜ฏ-๐˜ค๐˜ฐ๐˜ฏ๐˜ต๐˜ข๐˜ช๐˜ฏ๐˜ช๐˜ฏ๐˜จ ๐˜ฉ๐˜ช๐˜จ๐˜ฉ๐˜ฆ๐˜ณ ๐˜ฐ๐˜ณ๐˜ฅ๐˜ฆ๐˜ณ ๐˜ณ๐˜ฆ๐˜ด๐˜ท๐˜ฆ๐˜ณ๐˜ข๐˜ต๐˜ณ๐˜ฐ๐˜ญ ๐˜ฐ๐˜ญ๐˜ช๐˜จ๐˜ฐ๐˜ฎ๐˜ฆ๐˜ณ๐˜ด. Finally, this chapter describes our current studies towards more complex members of the resveratrol family. A concise approach for dihydrobenzofuran ring installation on the sevenmembered carbon framework of resveratrol-based oligomers is reported. The formation of 7,5- fused ring natural product cores ๐˜ท๐˜ช๐˜ข Friedel-Crafts cyclizations provides controlled access to some of the highly complex architectures within the resveratrol family.

Author and committee

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Author dc:creator
  • Lin, Yunqing

Subjects

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Rights

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English

Identifiers

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OAI identifier oai:identifier
oai:academiccommons.columbia.edu:10.7916/D8CF9X2D

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Columbia University
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academiccommons.columbia.edu/oai
Last updated
2026-07-24
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citation

Lin, Yunqing. Studies towards Selective Synthesis of Resveratrol-based Oligomeric Natural Products. 2011. https://doi.org/10.7916/D8CF9X2D