Issue 14, 2009
From the journal:

Chemical Communications

The first total synthesis of moracin O and moracin P, and establishment of the absolute configuration of moracin O†

Navneet Kaur,‡a   Yan Xia,‡a   Yinglan Jin,a   Nguyen Tien Dat,a   Kondaji Gajulapati,b   Yongseok Choi,b   Young-Soo Hong,a   Jung Joon Leea  and  Kyeong Lee*a  

* Corresponding authors

a Molecular Cancer Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 52 Eoeun-dong, Yuseong-gu, Korea
E-mail: kaylee@kribb.re.kr
Fax: +82 42 860 4595
Tel: +82 42 860 4382

b School of Life sciences and Biotechnology, Korea University, Anam-dong, Seongbuk-gu, Korea

Abstract

The first total synthesis of the naturally occurring benzofurans, moracins O and P was achieved using a Sonogashira cross coupling reaction followed by in situ cyclization, and the absolute configuration of natural moracin O was established.

Graphical abstract: The first total synthesis of moracin O and moracin P, and establishment of the absolute configuration of moracin O

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DOI
https://doi.org/10.1039/B823340C
Article type
Communication
Submitted
05 Jan 2009
Accepted
10 Feb 2009
First published
04 Mar 2009

Chem. Commun., 2009, 1879-1881

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The first total synthesis of moracin O and moracin P, and establishment of the absolute configuration of moracin O

N. Kaur, Y. Xia, Y. Jin, N. T. Dat, K. Gajulapati, Y. Choi, Y. Hong, J. J. Lee and K. Lee, Chem. Commun., 2009, 1879 DOI: 10.1039/B823340C

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