Application of a new nucleophilic addition/ring closure (NARC) sequence to the synthesis of enantiomerically-pure 2,8-dioxabicyclo[3.2.1]octanes of relevance to the squalestatins and zaragozic acids

Gary D Fallon; Eric Dale Jones; Patrick Perlmutter; Walailak Selajarern

Application of a new nucleophilic addition/ring closure (NARC) sequence to the synthesis of enantiomerically-pure 2,8-dioxabicyclo[3.2.1]octanes of relevance to the squalestatins and zaragozic acids

Gary D Fallon, Eric Dale Jones, Patrick Perlmutter, Walailak Selajarern

School of Chemistry

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

16 Citations (Scopus)

Abstract

A rapid method for the enantioselective construction of 2,8-dioxabicyclo[3.2.1]octanes of relevance to the zaragozic acids, employing a tandem NARC sequence of aldol and intramol. Wacker reactions, is described. [on SciFinder(R)]

Original language	English
Pages (from-to)	7435 - 7438
Number of pages	4
Journal	Tetrahedron Letters
Volume	40
Issue number	41
Publication status	Published - 1999

Cite this

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title = "Application of a new nucleophilic addition/ring closure (NARC) sequence to the synthesis of enantiomerically-pure 2,8-dioxabicyclo[3.2.1]octanes of relevance to the squalestatins and zaragozic acids",

abstract = "A rapid method for the enantioselective construction of 2,8-dioxabicyclo[3.2.1]octanes of relevance to the zaragozic acids, employing a tandem NARC sequence of aldol and intramol. Wacker reactions, is described. [on SciFinder(R)]",

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year = "1999",

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journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "41",

}

Application of a new nucleophilic addition/ring closure (NARC) sequence to the synthesis of enantiomerically-pure 2,8-dioxabicyclo[3.2.1]octanes of relevance to the squalestatins and zaragozic acids. / Fallon, Gary D; Jones, Eric Dale; Perlmutter, Patrick et al.
In: Tetrahedron Letters, Vol. 40, No. 41, 1999, p. 7435 - 7438.

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

TY - JOUR

T1 - Application of a new nucleophilic addition/ring closure (NARC) sequence to the synthesis of enantiomerically-pure 2,8-dioxabicyclo[3.2.1]octanes of relevance to the squalestatins and zaragozic acids

AU - Fallon, Gary D

AU - Jones, Eric Dale

AU - Perlmutter, Patrick

AU - Selajarern, Walailak

PY - 1999

Y1 - 1999

N2 - A rapid method for the enantioselective construction of 2,8-dioxabicyclo[3.2.1]octanes of relevance to the zaragozic acids, employing a tandem NARC sequence of aldol and intramol. Wacker reactions, is described. [on SciFinder(R)]

AB - A rapid method for the enantioselective construction of 2,8-dioxabicyclo[3.2.1]octanes of relevance to the zaragozic acids, employing a tandem NARC sequence of aldol and intramol. Wacker reactions, is described. [on SciFinder(R)]

UR - http://tinyurl.com/zw3c2ck

M3 - Article

SN - 0040-4039

VL - 40

SP - 7435

EP - 7438

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 41

ER -

Application of a new nucleophilic addition/ring closure (NARC) sequence to the synthesis of enantiomerically-pure 2,8-dioxabicyclo[3.2.1]octanes of relevance to the squalestatins and zaragozic acids

Abstract

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