Enantioselective formal synthesis of antitumor agent (+)-ottelione A

Mi Young Lee; Kyung Hwa Kim; Shuai Jiang; Yoo Hyun Jung; Jae Yi Sim; Geum Sook Hwang; Do Hyun Ryu

doi:10.1016/j.tetlet.2008.01.108

Enantioselective formal synthesis of antitumor agent (+)-ottelione A

Mi Young Lee
, Kyung Hwa Kim
, Shuai Jiang
, Yoo Hyun Jung
, Jae Yi Sim
, Geum Sook Hwang
, Do Hyun Ryu

Department of Chemistry

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

23 Scopus citations

Abstract

The enantioselective formal synthesis of a natural antitumor product, (+)-ottelione A, was achieved through a catalytic enantioselective Diels-Alder strategy. These endeavors have led to the synthesis of a variety of synthetic analogues of this biologically potent natural product.

Original language	English
Pages (from-to)	1965-1967
Number of pages	3
Journal	Tetrahedron Letters
Volume	49
Issue number	12
DOIs	https://doi.org/10.1016/j.tetlet.2008.01.108
State	Published - 17 Mar 2008

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10.1016/j.tetlet.2008.01.108

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title = "Enantioselective formal synthesis of antitumor agent (+)-ottelione A",

abstract = "The enantioselective formal synthesis of a natural antitumor product, (+)-ottelione A, was achieved through a catalytic enantioselective Diels-Alder strategy. These endeavors have led to the synthesis of a variety of synthetic analogues of this biologically potent natural product.",

author = "Lee, \{Mi Young\} and Kim, \{Kyung Hwa\} and Shuai Jiang and Jung, \{Yoo Hyun\} and Sim, \{Jae Yi\} and Hwang, \{Geum Sook\} and Ryu, \{Do Hyun\}",

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AU - Lee, Mi Young

AU - Kim, Kyung Hwa

AU - Jiang, Shuai

AU - Jung, Yoo Hyun

AU - Sim, Jae Yi

AU - Hwang, Geum Sook

AU - Ryu, Do Hyun

PY - 2008/3/17

Y1 - 2008/3/17

N2 - The enantioselective formal synthesis of a natural antitumor product, (+)-ottelione A, was achieved through a catalytic enantioselective Diels-Alder strategy. These endeavors have led to the synthesis of a variety of synthetic analogues of this biologically potent natural product.

AB - The enantioselective formal synthesis of a natural antitumor product, (+)-ottelione A, was achieved through a catalytic enantioselective Diels-Alder strategy. These endeavors have led to the synthesis of a variety of synthetic analogues of this biologically potent natural product.

UR - https://www.scopus.com/pages/publications/39549121796

U2 - 10.1016/j.tetlet.2008.01.108

DO - 10.1016/j.tetlet.2008.01.108

M3 - Article

AN - SCOPUS:39549121796

SN - 0040-4039

VL - 49

SP - 1965

EP - 1967

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 12

ER -

Enantioselective formal synthesis of antitumor agent (+)-ottelione A

Abstract

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