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Synthesis of the erythrina alkaloid 3-demethoxyerythratidinone. Novel acid-induced rearrangements of its precursors.

Publication ,  Journal Article
Wang, Q; Padwa, A
Published in: Organic letters
February 2006

[reaction: see text] A new strategy for the synthesis of 3-demethoxyerythratidinone has been developed and is based on an extraordinarily facile intramolecular Diels-Alder reaction of a 2-imido-substituted furan. During the course of the synthesis, several novel acid-induced rearrangement reactions were encountered.

Duke Scholars

Published In

Organic letters

DOI

EISSN

1523-7052

ISSN

1523-7060

Publication Date

February 2006

Volume

8

Issue

4

Start / End Page

601 / 604

Related Subject Headings

  • Organic Chemistry
  • Molecular Structure
  • Indole Alkaloids
  • Indicators and Reagents
  • Erythrina
  • Catalysis
  • 34 Chemical sciences
  • 03 Chemical Sciences
 

Citation

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ICMJE
MLA
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Wang, Q., & Padwa, A. (2006). Synthesis of the erythrina alkaloid 3-demethoxyerythratidinone. Novel acid-induced rearrangements of its precursors. Organic Letters, 8(4), 601–604. https://doi.org/10.1021/ol0527330
Wang, Qiu, and Albert Padwa. “Synthesis of the erythrina alkaloid 3-demethoxyerythratidinone. Novel acid-induced rearrangements of its precursors.Organic Letters 8, no. 4 (February 2006): 601–4. https://doi.org/10.1021/ol0527330.
Wang, Qiu, and Albert Padwa. “Synthesis of the erythrina alkaloid 3-demethoxyerythratidinone. Novel acid-induced rearrangements of its precursors.Organic Letters, vol. 8, no. 4, Feb. 2006, pp. 601–04. Epmc, doi:10.1021/ol0527330.
Journal cover image

Published In

Organic letters

DOI

EISSN

1523-7052

ISSN

1523-7060

Publication Date

February 2006

Volume

8

Issue

4

Start / End Page

601 / 604

Related Subject Headings

  • Organic Chemistry
  • Molecular Structure
  • Indole Alkaloids
  • Indicators and Reagents
  • Erythrina
  • Catalysis
  • 34 Chemical sciences
  • 03 Chemical Sciences