Selective cycloalkanone reductions using aluminum amalgam

Martin Hulce; Timothy LaVaute

doi:10.1016/S0040-4039(00)80139-2

Selective cycloalkanone reductions using aluminum amalgam

Martin Hulce, Timothy LaVaute

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

26 Scopus citations

Abstract

Aluminum amalgam in aqueous tetrahydrofuran reduces cycloalkanones to their respective alcohols. The reaction exhibits sensitivity to the ring size and steric environment of the ketone.

Original language	English (US)
Pages (from-to)	525-528
Number of pages	4
Journal	Tetrahedron Letters
Volume	29
Issue number	5
DOIs	https://doi.org/10.1016/S0040-4039(00)80139-2
State	Published - 1988
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)80139-2

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@article{97dacae134504d5cbf94be66075a60d2,

title = "Selective cycloalkanone reductions using aluminum amalgam",

abstract = "Aluminum amalgam in aqueous tetrahydrofuran reduces cycloalkanones to their respective alcohols. The reaction exhibits sensitivity to the ring size and steric environment of the ketone.",

author = "Martin Hulce and Timothy LaVaute",

note = "Funding Information: Acknowledgement. Acknowledgement is made to the Donors of the Petroleum Research Fund, administered by the American Chemical Society, for partial support of this research.",

year = "1988",

doi = "10.1016/S0040-4039(00)80139-2",

language = "English (US)",

volume = "29",

pages = "525--528",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "5",

}

TY - JOUR

T1 - Selective cycloalkanone reductions using aluminum amalgam

AU - Hulce, Martin

AU - LaVaute, Timothy

N1 - Funding Information: Acknowledgement. Acknowledgement is made to the Donors of the Petroleum Research Fund, administered by the American Chemical Society, for partial support of this research.

PY - 1988

Y1 - 1988

N2 - Aluminum amalgam in aqueous tetrahydrofuran reduces cycloalkanones to their respective alcohols. The reaction exhibits sensitivity to the ring size and steric environment of the ketone.

AB - Aluminum amalgam in aqueous tetrahydrofuran reduces cycloalkanones to their respective alcohols. The reaction exhibits sensitivity to the ring size and steric environment of the ketone.

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UR - http://www.scopus.com/inward/citedby.url?scp=0000957482&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)80139-2

DO - 10.1016/S0040-4039(00)80139-2

M3 - Article

AN - SCOPUS:0000957482

VL - 29

SP - 525

EP - 528

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 5

ER -

Selective cycloalkanone reductions using aluminum amalgam

Abstract

All Science Journal Classification (ASJC) codes

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