Facile synthesis of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives via a domino Knoevenagel condensation/hetero-Diels-Alder reaction sequence

Ikyon Kim; Sun Gi Kim; Jihyun Choi; Ge Hyeong Lee

doi:10.1016/j.tet.2007.11.036

Facile synthesis of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives via a domino Knoevenagel condensation/hetero-Diels-Alder reaction sequence

Ikyon Kim, Sun Gi Kim, Jihyun Choi, Ge Hyeong Lee

Department of Pharmacy

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

58 Citations (Scopus)

Abstract

A facile two-step synthesis of a series of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives is described, featuring a domino Knoevenagel condensation/intramolecular hetero-Diels-Alder reaction sequence.

Original language	English
Pages (from-to)	664-671
Number of pages	8
Journal	Tetrahedron
Volume	64
Issue number	4
DOIs	https://doi.org/10.1016/j.tet.2007.11.036
Publication status	Published - 2008 Jan 21

Bibliographical note

Funding Information:
We thank the Center for Biological Modulators and Korea Research Institute of Chemical Technology for generous financial support.

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tet.2007.11.036

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title = "Facile synthesis of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives via a domino Knoevenagel condensation/hetero-Diels-Alder reaction sequence",

abstract = "A facile two-step synthesis of a series of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives is described, featuring a domino Knoevenagel condensation/intramolecular hetero-Diels-Alder reaction sequence.",

author = "Ikyon Kim and Kim, {Sun Gi} and Jihyun Choi and Lee, {Ge Hyeong}",

note = "Funding Information: We thank the Center for Biological Modulators and Korea Research Institute of Chemical Technology for generous financial support. ",

year = "2008",

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day = "21",

doi = "10.1016/j.tet.2007.11.036",

language = "English",

volume = "64",

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T1 - Facile synthesis of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives via a domino Knoevenagel condensation/hetero-Diels-Alder reaction sequence

AU - Kim, Ikyon

AU - Kim, Sun Gi

AU - Choi, Jihyun

AU - Lee, Ge Hyeong

N1 - Funding Information: We thank the Center for Biological Modulators and Korea Research Institute of Chemical Technology for generous financial support.

PY - 2008/1/21

Y1 - 2008/1/21

N2 - A facile two-step synthesis of a series of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives is described, featuring a domino Knoevenagel condensation/intramolecular hetero-Diels-Alder reaction sequence.

AB - A facile two-step synthesis of a series of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives is described, featuring a domino Knoevenagel condensation/intramolecular hetero-Diels-Alder reaction sequence.

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U2 - 10.1016/j.tet.2007.11.036

DO - 10.1016/j.tet.2007.11.036

M3 - Article

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VL - 64

SP - 664

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JO - Tetrahedron

JF - Tetrahedron

IS - 4

ER -

Facile synthesis of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives via a domino Knoevenagel condensation/hetero-Diels-Alder reaction sequence

Abstract

Bibliographical note

All Science Journal Classification (ASJC) codes

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