The NARC-based approach to the enantioselective synthesis of the zaragozic acids. Synthesis of a C 5-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octane

Patrick Perlmutter; Walailak Selajarern

doi:10.1071/CH00045

The NARC-based approach to the enantioselective synthesis of the zaragozic acids. Synthesis of a C 5-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octane

Patrick Perlmutter
, Walailak Selajarern

School of Chemistry

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

Abstract

A direct method for the prepn. of C(5)-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octanes is described. The key process involves a highly stereoselective NARC sequence of a nucleophilic addn. followed by ring closure. [on SciFinder(R)]

Original language	English
Pages (from-to)	349 - 353
Number of pages	5
Journal	Australian Journal of Chemistry
Volume	53
Issue number	4
DOIs	https://doi.org/10.1071/CH00045
Publication status	Published - 2000

Access to Document

10.1071/CH00045

Cite this

@article{7a44b5afa16b493fa7961b474fd3a550,

title = "The NARC-based approach to the enantioselective synthesis of the zaragozic acids. Synthesis of a C 5-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octane",

abstract = "A direct method for the prepn. of C(5)-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octanes is described. The key process involves a highly stereoselective NARC sequence of a nucleophilic addn. followed by ring closure. [on SciFinder(R)]",

author = "Patrick Perlmutter and Walailak Selajarern",

year = "2000",

doi = "10.1071/CH00045",

language = "English",

volume = "53",

pages = "349 -- 353",

journal = "Australian Journal of Chemistry",

issn = "1445-0038",

publisher = "CSIRO Publishing",

number = "4",

}

TY - JOUR

T1 - The NARC-based approach to the enantioselective synthesis of the zaragozic acids. Synthesis of a C 5-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octane

AU - Perlmutter, Patrick

AU - Selajarern, Walailak

PY - 2000

Y1 - 2000

N2 - A direct method for the prepn. of C(5)-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octanes is described. The key process involves a highly stereoselective NARC sequence of a nucleophilic addn. followed by ring closure. [on SciFinder(R)]

AB - A direct method for the prepn. of C(5)-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octanes is described. The key process involves a highly stereoselective NARC sequence of a nucleophilic addn. followed by ring closure. [on SciFinder(R)]

UR - http://www.publish.csiro.au/?act=view_file&file_id=CH00045.pdf

U2 - 10.1071/CH00045

DO - 10.1071/CH00045

M3 - Article

SN - 1445-0038

VL - 53

SP - 349

EP - 353

JO - Australian Journal of Chemistry

JF - Australian Journal of Chemistry

IS - 4

ER -

The NARC-based approach to the enantioselective synthesis of the zaragozic acids. Synthesis of a C 5-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octane

Abstract

Access to Document

Other files and links

Cite this