Exploration of the "traceless" reductive ligation of S-nitrosothiols

Jiming Zhang, Hua Wang, Ming Xian

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

(Chemical Equation Presented) The first "traceless" reductive ligation of S-nitrosothiols using phosphine ester/thioester conjugates is reported. Experiments also show that stable thiolmidate compounds could be formed in the reaction between S-nitrosothiols and some phosphine-thioester substrates.

Original languageEnglish (US)
Pages (from-to)477-480
Number of pages4
JournalOrganic Letters
Volume11
Issue number2
DOIs
StatePublished - Jan 15 2009
Externally publishedYes

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phosphine
S-Nitrosothiols
phosphines
Ligation
esters
Esters
Substrates
Experiments

ASJC Scopus subject areas

  • Organic Chemistry
  • Physical and Theoretical Chemistry
  • Biochemistry

Cite this

Exploration of the "traceless" reductive ligation of S-nitrosothiols. / Zhang, Jiming; Wang, Hua; Xian, Ming.

In: Organic Letters, Vol. 11, No. 2, 15.01.2009, p. 477-480.

Research output: Contribution to journalArticle

Zhang, Jiming ; Wang, Hua ; Xian, Ming. / Exploration of the "traceless" reductive ligation of S-nitrosothiols. In: Organic Letters. 2009 ; Vol. 11, No. 2. pp. 477-480.
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