Iron catalysed selective reduction of esters to alcohols

Sem Raj Tamang; Anthony F. Cozzolino; Michael Findlater

doi:10.1039/c8ob02661k

Iron catalysed selective reduction of esters to alcohols

Sem Raj Tamang, Anthony F. Cozzolino, Michael Findlater

Chemistry and Biochemistry

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

8 Scopus citations

Abstract

The reaction of (dppBIAN)FeCl ₂ with 3 equivalents of n-BuLi affords a catalytically active anionic Fe complex; the nature of the anionic complex was probed using EPR and IR experiments and is proposed to involve a dearomatized, radical, ligand scaffold. This complex is an active catalyst for the hydrosilylation of esters to afford alcohols; loadings as low as 1 mol% were employed.

Original language	English
Pages (from-to)	1834-1838
Number of pages	5
Journal	Organic and Biomolecular Chemistry
Volume	17
Issue number	7
DOIs	https://doi.org/10.1039/c8ob02661k
State	Published - 2019

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title = "Iron catalysed selective reduction of esters to alcohols",

abstract = " The reaction of (dppBIAN)FeCl 2 with 3 equivalents of n-BuLi affords a catalytically active anionic Fe complex; the nature of the anionic complex was probed using EPR and IR experiments and is proposed to involve a dearomatized, radical, ligand scaffold. This complex is an active catalyst for the hydrosilylation of esters to afford alcohols; loadings as low as 1 mol% were employed. ",

author = "Tamang, {Sem Raj} and Cozzolino, {Anthony F.} and Michael Findlater",

note = "Funding Information: The financial support of the Robert A. Welch Foundation is gratefully acknowledged (Grant No. D1807). Dr Anne-Marie Dechert-Schmitt is thanked for helpful discussions and comments on an earlier draft of this manuscript. Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2019.",

year = "2019",

doi = "10.1039/c8ob02661k",

language = "English",

volume = "17",

pages = "1834--1838",

journal = "Organic and Biomolecular Chemistry",

issn = "1477-0520",

number = "7",

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T1 - Iron catalysed selective reduction of esters to alcohols

AU - Tamang, Sem Raj

AU - Cozzolino, Anthony F.

AU - Findlater, Michael

N1 - Funding Information: The financial support of the Robert A. Welch Foundation is gratefully acknowledged (Grant No. D1807). Dr Anne-Marie Dechert-Schmitt is thanked for helpful discussions and comments on an earlier draft of this manuscript. Publisher Copyright: © The Royal Society of Chemistry 2019.

PY - 2019

Y1 - 2019

N2 - The reaction of (dppBIAN)FeCl 2 with 3 equivalents of n-BuLi affords a catalytically active anionic Fe complex; the nature of the anionic complex was probed using EPR and IR experiments and is proposed to involve a dearomatized, radical, ligand scaffold. This complex is an active catalyst for the hydrosilylation of esters to afford alcohols; loadings as low as 1 mol% were employed.

AB - The reaction of (dppBIAN)FeCl 2 with 3 equivalents of n-BuLi affords a catalytically active anionic Fe complex; the nature of the anionic complex was probed using EPR and IR experiments and is proposed to involve a dearomatized, radical, ligand scaffold. This complex is an active catalyst for the hydrosilylation of esters to afford alcohols; loadings as low as 1 mol% were employed.

UR - http://www.scopus.com/inward/record.url?scp=85061511676&partnerID=8YFLogxK

U2 - 10.1039/c8ob02661k

DO - 10.1039/c8ob02661k

M3 - Article

C2 - 30604820

AN - SCOPUS:85061511676

VL - 17

SP - 1834

EP - 1838

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

SN - 1477-0520

IS - 7

ER -

Iron catalysed selective reduction of esters to alcohols

Abstract

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