Selenofluorenone: Synthesis and cycloaddition chemistry

Peter T. Meinke; Grant A. Krafft; James T. Spencer

doi:10.1016/S0040-4039(00)96411-6

Selenofluorenone: Synthesis and cycloaddition chemistry

Peter T. Meinke, Grant A. Krafft, James T. Spencer

Department of Chemistry

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

21 Scopus citations

Abstract

Selenofluorenone, prepared from fluorenyl selenocyanate by base-induced elimination, participates efficiently in Diels-Alder cycloaddition and 1,3-dipolar cycloaddition reactions.

Original language	English (US)
Pages (from-to)	3887-3890
Number of pages	4
Journal	Tetrahedron Letters
Volume	28
Issue number	34
DOIs	https://doi.org/10.1016/S0040-4039(00)96411-6
State	Published - 1987

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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title = "Selenofluorenone: Synthesis and cycloaddition chemistry",

abstract = "Selenofluorenone, prepared from fluorenyl selenocyanate by base-induced elimination, participates efficiently in Diels-Alder cycloaddition and 1,3-dipolar cycloaddition reactions.",

author = "Meinke, {Peter T.} and Krafft, {Grant A.} and Spencer, {James T.}",

year = "1987",

doi = "10.1016/S0040-4039(00)96411-6",

language = "English (US)",

volume = "28",

pages = "3887--3890",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "34",

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TY - JOUR

T1 - Selenofluorenone

T2 - Synthesis and cycloaddition chemistry

AU - Meinke, Peter T.

AU - Krafft, Grant A.

AU - Spencer, James T.

PY - 1987

Y1 - 1987

N2 - Selenofluorenone, prepared from fluorenyl selenocyanate by base-induced elimination, participates efficiently in Diels-Alder cycloaddition and 1,3-dipolar cycloaddition reactions.

AB - Selenofluorenone, prepared from fluorenyl selenocyanate by base-induced elimination, participates efficiently in Diels-Alder cycloaddition and 1,3-dipolar cycloaddition reactions.

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U2 - 10.1016/S0040-4039(00)96411-6

DO - 10.1016/S0040-4039(00)96411-6

M3 - Article

AN - SCOPUS:0342816913

SN - 0040-4039

VL - 28

SP - 3887

EP - 3890

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 34

ER -

Selenofluorenone: Synthesis and cycloaddition chemistry

Abstract

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