Total Syntheses of Urgineanins A, B, D, and Their Analogues

Dileep Kumar Singh, Youngeun Jung, Ikyon Kim

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

The first asymmetric total syntheses of urgineanins A, B, and D - potent antiproliferative homoisoflavonoids - were achieved by utilizing Pd-catalyzed allylic substitution of the allylic acetate with arylboronic acids for introduction of the C rings of homoisoflavonoid skeleton. Several unnatural urgineanin analogues were also prepared in this manner.

Original languageEnglish
Article numberss-2016-h0625-op
Pages (from-to)1531-1537
Number of pages7
JournalSynthesis (Germany)
Volume49
Issue number7
DOIs
Publication statusPublished - 2017 Apr 1

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Acetates
Substitution reactions
Acids

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Organic Chemistry

Cite this

Singh, Dileep Kumar ; Jung, Youngeun ; Kim, Ikyon. / Total Syntheses of Urgineanins A, B, D, and Their Analogues. In: Synthesis (Germany). 2017 ; Vol. 49, No. 7. pp. 1531-1537.
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Total Syntheses of Urgineanins A, B, D, and Their Analogues. / Singh, Dileep Kumar; Jung, Youngeun; Kim, Ikyon.

In: Synthesis (Germany), Vol. 49, No. 7, ss-2016-h0625-op, 01.04.2017, p. 1531-1537.

Research output: Contribution to journalArticle

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