Synthesis of (±)-Panduratin A and related natural products using the high pressure diels-alder reaction

Luke A. Pasfield; Laura delaCruz; Junming Ho; Michelle L. Coote; Gottfried Otting; Malcolm D. Mcleod

doi:10.1002/ajoc.201200171

Synthesis of (±)-Panduratin A and related natural products using the high pressure diels-alder reaction

Luke A. Pasfield, Laura delaCruz, Junming Ho, Michelle L. Coote, Gottfried Otting, Malcolm D. Mcleod^*

^*Corresponding author for this work

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

17 Citations (Scopus)

Abstract

Under pressure: PanduratinA (1) has been synthesized in six steps including a high pressure Diels-Alder reaction. This divergent sequence also allowed the synthesis of 4-hydroxypanduratinA, panduratinH, panduratinI, nicolaioidesinB, and 2-hydroxyisopanduratinA. The binding of panduratinA to the dengue virus NS2B-NS3 protease was investigated by NMR spectroscopy.

Original language	English
Pages (from-to)	60-63
Number of pages	4
Journal	Asian Journal of Organic Chemistry
Volume	2
Issue number	1
DOIs	https://doi.org/10.1002/ajoc.201200171
Publication status	Published - Jan 2013

Access to Document

10.1002/ajoc.201200171

Cite this

@article{54dc9671ef0042d19b45f40d096dbf6e,

title = "Synthesis of (±)-Panduratin A and related natural products using the high pressure diels-alder reaction",

abstract = "Under pressure: PanduratinA (1) has been synthesized in six steps including a high pressure Diels-Alder reaction. This divergent sequence also allowed the synthesis of 4-hydroxypanduratinA, panduratinH, panduratinI, nicolaioidesinB, and 2-hydroxyisopanduratinA. The binding of panduratinA to the dengue virus NS2B-NS3 protease was investigated by NMR spectroscopy.",

keywords = "Dengue virus, High-pressure chemistry, Natural products, Protein NMR, Total synthesis",

author = "Pasfield, {Luke A.} and Laura delaCruz and Junming Ho and Coote, {Michelle L.} and Gottfried Otting and Mcleod, {Malcolm D.}",

year = "2013",

month = jan,

doi = "10.1002/ajoc.201200171",

language = "English",

volume = "2",

pages = "60--63",

journal = "Asian Journal of Organic Chemistry",

issn = "2193-5807",

publisher = "Wiley-VCH Verlag GmbH",

number = "1",

}

TY - JOUR

T1 - Synthesis of (±)-Panduratin A and related natural products using the high pressure diels-alder reaction

AU - Pasfield, Luke A.

AU - delaCruz, Laura

AU - Ho, Junming

AU - Coote, Michelle L.

AU - Otting, Gottfried

AU - Mcleod, Malcolm D.

PY - 2013/1

Y1 - 2013/1

N2 - Under pressure: PanduratinA (1) has been synthesized in six steps including a high pressure Diels-Alder reaction. This divergent sequence also allowed the synthesis of 4-hydroxypanduratinA, panduratinH, panduratinI, nicolaioidesinB, and 2-hydroxyisopanduratinA. The binding of panduratinA to the dengue virus NS2B-NS3 protease was investigated by NMR spectroscopy.

AB - Under pressure: PanduratinA (1) has been synthesized in six steps including a high pressure Diels-Alder reaction. This divergent sequence also allowed the synthesis of 4-hydroxypanduratinA, panduratinH, panduratinI, nicolaioidesinB, and 2-hydroxyisopanduratinA. The binding of panduratinA to the dengue virus NS2B-NS3 protease was investigated by NMR spectroscopy.

KW - Dengue virus

KW - High-pressure chemistry

KW - Natural products

KW - Protein NMR

KW - Total synthesis

UR - http://www.scopus.com/inward/record.url?scp=84899740484&partnerID=8YFLogxK

U2 - 10.1002/ajoc.201200171

DO - 10.1002/ajoc.201200171

M3 - Article

SN - 2193-5807

VL - 2

SP - 60

EP - 63

JO - Asian Journal of Organic Chemistry

JF - Asian Journal of Organic Chemistry

IS - 1

ER -

Synthesis of (±)-Panduratin A and related natural products using the high pressure diels-alder reaction

Abstract

Access to Document

Other files and links

Fingerprint

Cite this