Synthesis of the C1-C16 fragment of the ajudazols

B A Egan; M Paradowski; Lynne H Thomas; R Marquez

doi:10.1016/j.tet.2011.10.036

Synthesis of the C1-C16 fragment of the ajudazols

B A Egan, M Paradowski, Lynne H Thomas, R Marquez

Department of Chemistry

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

16 Citations (SciVal)

Abstract

The synthesis of the C1-C16 framework of the ajudazols has been achieved taking advantage of a highly selective isobenzofuran oxidative rearrangement and a key Stille coupling to introduce the key C14-C15 bond.

Original language	English
Pages (from-to)	9700-9707
Number of pages	8
Journal	Tetrahedron
Volume	67
Issue number	50
DOIs	https://doi.org/10.1016/j.tet.2011.10.036
Publication status	Published - 16 Dec 2011

Keywords

oxidative rearrangement
isobenzofuran
ajudazol

Access to Document

10.1016/j.tet.2011.10.036

Cite this

@article{e50762403462408eb055bf1531f340f4,

title = "Synthesis of the C1-C16 fragment of the ajudazols",

abstract = "The synthesis of the C1-C16 framework of the ajudazols has been achieved taking advantage of a highly selective isobenzofuran oxidative rearrangement and a key Stille coupling to introduce the key C14-C15 bond.",

keywords = "oxidative rearrangement, isobenzofuran, ajudazol",

author = "Egan, {B A} and M Paradowski and Thomas, {Lynne H} and R Marquez",

year = "2011",

month = dec,

day = "16",

doi = "10.1016/j.tet.2011.10.036",

language = "English",

volume = "67",

pages = "9700--9707",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier",

number = "50",

}

TY - JOUR

T1 - Synthesis of the C1-C16 fragment of the ajudazols

AU - Egan, B A

AU - Paradowski, M

AU - Thomas, Lynne H

AU - Marquez, R

PY - 2011/12/16

Y1 - 2011/12/16

N2 - The synthesis of the C1-C16 framework of the ajudazols has been achieved taking advantage of a highly selective isobenzofuran oxidative rearrangement and a key Stille coupling to introduce the key C14-C15 bond.

AB - The synthesis of the C1-C16 framework of the ajudazols has been achieved taking advantage of a highly selective isobenzofuran oxidative rearrangement and a key Stille coupling to introduce the key C14-C15 bond.

KW - oxidative rearrangement

KW - isobenzofuran

KW - ajudazol

UR - http://www.scopus.com/inward/record.url?scp=80655123146&partnerID=8YFLogxK

UR - http://dx.doi.org/10.1016/j.tet.2011.10.036

U2 - 10.1016/j.tet.2011.10.036

DO - 10.1016/j.tet.2011.10.036

M3 - Article

SN - 0040-4020

VL - 67

SP - 9700

EP - 9707

JO - Tetrahedron

JF - Tetrahedron

IS - 50

ER -

Synthesis of the C1-C16 fragment of the ajudazols

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Avance III 500 MHz Nuclear Magnetic Resonance (NMR) Spectrometer (9West)

Avance NEO 500 MHz Nuclear Magnetic Resonance (NMR) Spectrometer (1South)

Cite this

Synthesis of the C1-C16 fragment of the ajudazols

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Equipment

Avance III 500 MHz Nuclear Magnetic Resonance (NMR) Spectrometer (9West)

Avance NEO 500 MHz Nuclear Magnetic Resonance (NMR) Spectrometer (1South)

Cite this