A versatile approach to flavones via a one-pot Pd(II)-catalyzed dehydrogenation/oxidative boron-Heck coupling sequence of chromanones

Jun Lee; Jihyun Yu; Seung Hwan Son; Jinyuk Heo; Taelim Kim; Ji Young An; Kyung Soo Inn; Nam Jung Kim

doi:10.1039/c5ob01911g

A versatile approach to flavones via a one-pot Pd(II)-catalyzed dehydrogenation/oxidative boron-Heck coupling sequence of chromanones

Jun Lee
, Jihyun Yu
, Seung Hwan Son
, Jinyuk Heo
, Taelim Kim
, Ji Young An
, Kyung Soo Inn
, Nam Jung Kim

Research output: Contribution to journal › Article › peer-review

37 Citations (Scopus)

Abstract

A variety of flavones were expediently synthesized from readily accessible chromanones via a one-pot sequence involving Pd(ii)-catalyzed dehydrogenation and oxidative boron-Heck coupling with arylboronic acid pinacol esters. In particular, the use of arylboronic acid pinacol esters was found to significantly improve the yield of the reaction.

Original language	English
Pages (from-to)	777-784
Number of pages	8
Journal	Organic and Biomolecular Chemistry
Volume	14
Issue number	2
DOIs	https://doi.org/10.1039/c5ob01911g
Publication status	Published - 2016

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© 2016 The Royal Society of Chemistry.

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10.1039/c5ob01911g

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abstract = "A variety of flavones were expediently synthesized from readily accessible chromanones via a one-pot sequence involving Pd(ii)-catalyzed dehydrogenation and oxidative boron-Heck coupling with arylboronic acid pinacol esters. In particular, the use of arylboronic acid pinacol esters was found to significantly improve the yield of the reaction.",

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AU - Lee, Jun

AU - Yu, Jihyun

AU - Son, Seung Hwan

AU - Heo, Jinyuk

AU - Kim, Taelim

AU - An, Ji Young

AU - Inn, Kyung Soo

AU - Kim, Nam Jung

PY - 2016

Y1 - 2016

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AB - A variety of flavones were expediently synthesized from readily accessible chromanones via a one-pot sequence involving Pd(ii)-catalyzed dehydrogenation and oxidative boron-Heck coupling with arylboronic acid pinacol esters. In particular, the use of arylboronic acid pinacol esters was found to significantly improve the yield of the reaction.

UR - https://www.scopus.com/pages/publications/84953329977

U2 - 10.1039/c5ob01911g

DO - 10.1039/c5ob01911g

M3 - Article

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AN - SCOPUS:84953329977

SN - 1477-0520

VL - 14

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EP - 784

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

IS - 2

ER -

A versatile approach to flavones via a one-pot Pd(II)-catalyzed dehydrogenation/oxidative boron-Heck coupling sequence of chromanones

Abstract

Bibliographical note

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