Progress toward the total synthesis of saudin: Development of a tandem Stille-oxa-electrocyclization reaction

Uttam K. Tambar; Taichi Kano; Brian M. Stoltz

doi:10.1021/ol050705b

Progress toward the total synthesis of saudin: Development of a tandem Stille-oxa-electrocyclization reaction

Uttam K. Tambar, Taichi Kano, Brian M. Stoltz

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

31 Scopus citations

Abstract

(Chemical Equation Presented) A diastereoselective tandem Stille-oxa-electrocyclization reaction provides access to the core of the diterpenoid natural product saudin. Additionally, this new reaction sequence was extended to the convergent preparation of related polycyclic pyran systems.

Original language	English (US)
Pages (from-to)	2413-2416
Number of pages	4
Journal	Organic Letters
Volume	7
Issue number	12
DOIs	https://doi.org/10.1021/ol050705b
State	Published - Jun 9 2005

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol050705b

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title = "Progress toward the total synthesis of saudin: Development of a tandem Stille-oxa-electrocyclization reaction",

abstract = "(Chemical Equation Presented) A diastereoselective tandem Stille-oxa-electrocyclization reaction provides access to the core of the diterpenoid natural product saudin. Additionally, this new reaction sequence was extended to the convergent preparation of related polycyclic pyran systems.",

author = "Tambar, {Uttam K.} and Taichi Kano and Stoltz, {Brian M.}",

year = "2005",

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doi = "10.1021/ol050705b",

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AU - Tambar, Uttam K.

AU - Kano, Taichi

AU - Stoltz, Brian M.

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Y1 - 2005/6/9

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AB - (Chemical Equation Presented) A diastereoselective tandem Stille-oxa-electrocyclization reaction provides access to the core of the diterpenoid natural product saudin. Additionally, this new reaction sequence was extended to the convergent preparation of related polycyclic pyran systems.

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JO - Organic Letters

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Progress toward the total synthesis of saudin: Development of a tandem Stille-oxa-electrocyclization reaction

Abstract

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