New Odorless Protocols for the Synthesis of Aldehydes and Ketones from Thiol Esters

Tohru Miyazaki; Yuki Han-Ya; Hidetoshi Tokuyama; Tohru Fukuyama

doi:10.1055/s-2004-815427

New Odorless Protocols for the Synthesis of Aldehydes and Ketones from Thiol Esters

Tohru Miyazaki, Yuki Han-Ya, Hidetoshi Tokuyama, Tohru Fukuyama

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

74 Citations (Scopus)

Abstract

Dodecanethiol esters derived from odorless dodecanethiol proved to be suitable substrates for Pd-catalyzed reduction with triethylsilane, coupling with organozinc reagents, and coupling with terminal acetylenes.

Original language	English
Pages (from-to)	477-480
Number of pages	4
Journal	Synlett
Issue number	3
DOIs	https://doi.org/10.1055/s-2004-815427
Publication status	Published - 2004 Feb 18
Externally published	Yes

Keywords

Aldehyde
Ketone
Odorless dodecanethiol
Palladium-catalyzed reaction
Thiol esters

ASJC Scopus subject areas

Organic Chemistry

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title = "New Odorless Protocols for the Synthesis of Aldehydes and Ketones from Thiol Esters",

abstract = "Dodecanethiol esters derived from odorless dodecanethiol proved to be suitable substrates for Pd-catalyzed reduction with triethylsilane, coupling with organozinc reagents, and coupling with terminal acetylenes.",

keywords = "Aldehyde, Ketone, Odorless dodecanethiol, Palladium-catalyzed reaction, Thiol esters",

author = "Tohru Miyazaki and Yuki Han-Ya and Hidetoshi Tokuyama and Tohru Fukuyama",

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AU - Miyazaki, Tohru

AU - Han-Ya, Yuki

AU - Tokuyama, Hidetoshi

AU - Fukuyama, Tohru

PY - 2004/2/18

Y1 - 2004/2/18

N2 - Dodecanethiol esters derived from odorless dodecanethiol proved to be suitable substrates for Pd-catalyzed reduction with triethylsilane, coupling with organozinc reagents, and coupling with terminal acetylenes.

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KW - Aldehyde

KW - Ketone

KW - Odorless dodecanethiol

KW - Palladium-catalyzed reaction

KW - Thiol esters

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