The NARC-Based Approach to the Enantioselective Synthesis of the Zaragozic Acids. Synthesis of a C5-Alkoxycarbonyl-Substituted 2,8-Dioxabicyclo[3.2.1]octane

Patrick P Perlmutter; Walailak Selajarern

The NARC-Based Approach to the Enantioselective Synthesis of the Zaragozic Acids. Synthesis of a C5-Alkoxycarbonyl-Substituted 2,8-Dioxabicyclo[3.2.1]octane

Patrick P Perlmutter
, Walailak Selajarern

School of Chemistry

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

Original language	English
Pages (from-to)	349 - 353
Number of pages	5
Journal	Australian Journal of Chemistry
Publication status	Published - 2000

Cite this

@article{2a29e3d1b7ed4a0793c261519c3cf0a7,

title = "The NARC-Based Approach to the Enantioselective Synthesis of the Zaragozic Acids. Synthesis of a C5-Alkoxycarbonyl-Substituted 2,8-Dioxabicyclo[3.2.1]octane",

author = "Perlmutter, \{Patrick P\} and Walailak Selajarern",

year = "2000",

language = "English",

pages = "349 -- 353",

journal = "Australian Journal of Chemistry",

issn = "1445-0038",

publisher = "CSIRO Publishing",

}

TY - JOUR

T1 - The NARC-Based Approach to the Enantioselective Synthesis of the Zaragozic Acids. Synthesis of a C5-Alkoxycarbonyl-Substituted 2,8-Dioxabicyclo[3.2.1]octane

AU - Perlmutter, Patrick P

AU - Selajarern, Walailak

PY - 2000

Y1 - 2000

M3 - Article

SN - 1445-0038

SP - 349

EP - 353

JO - Australian Journal of Chemistry

JF - Australian Journal of Chemistry

ER -