Selenocarbonyl synthesis using Woollins Reagent

Pravat Bhattacharyya; John Derek Woollins

doi:10.1016/S0040-4039(01)01113-3

Selenocarbonyl synthesis using Woollins Reagent

Pravat Bhattacharyya, John Derek Woollins

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

Abstract

[PhP(Se)(mu -Se)](2) selenates secondary and tertiary amides to the corresponding selenoamides in 30-70% yields at 130 degreesC in toluene and indolizine-3-aldehydes to selenoaldehydes in 40-59% yield at 25 degreesC. (C) 2001 Elsevier Science Ltd. All rights reserved.

Original language	English
Pages (from-to)	5949-5951
Journal	Tetrahedron Letters
Volume	42
Issue number	34
DOIs	https://doi.org/10.1016/S0040-4039(01)01113-3
Publication status	Published - 20 Aug 2001

Keywords

Selenoamide
Selenoaldehyde
Selenation
Woollins reagent
Telluroamides
Selenoamides
Selenide

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10.1016/S0040-4039(01)01113-3

Tetrahedronarticle
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title = "Selenocarbonyl synthesis using Woollins Reagent",

abstract = "[PhP(Se)(mu -Se)](2) selenates secondary and tertiary amides to the corresponding selenoamides in 30-70% yields at 130 degreesC in toluene and indolizine-3-aldehydes to selenoaldehydes in 40-59% yield at 25 degreesC. (C) 2001 Elsevier Science Ltd. All rights reserved.",

keywords = "Selenoamide, Selenoaldehyde, Selenation, Woollins reagent, Telluroamides, Selenoamides, Selenide",

author = "Pravat Bhattacharyya and Woollins, {John Derek}",

note = "This work was funded by EPSRC",

year = "2001",

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doi = "10.1016/S0040-4039(01)01113-3",

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T1 - Selenocarbonyl synthesis using Woollins Reagent

AU - Bhattacharyya, Pravat

AU - Woollins, John Derek

N1 - This work was funded by EPSRC

PY - 2001/8/20

Y1 - 2001/8/20

N2 - [PhP(Se)(mu -Se)](2) selenates secondary and tertiary amides to the corresponding selenoamides in 30-70% yields at 130 degreesC in toluene and indolizine-3-aldehydes to selenoaldehydes in 40-59% yield at 25 degreesC. (C) 2001 Elsevier Science Ltd. All rights reserved.

AB - [PhP(Se)(mu -Se)](2) selenates secondary and tertiary amides to the corresponding selenoamides in 30-70% yields at 130 degreesC in toluene and indolizine-3-aldehydes to selenoaldehydes in 40-59% yield at 25 degreesC. (C) 2001 Elsevier Science Ltd. All rights reserved.

KW - Selenoamide

KW - Selenoaldehyde

KW - Selenation

KW - Woollins reagent

KW - Telluroamides

KW - Selenoamides

KW - Selenide

U2 - 10.1016/S0040-4039(01)01113-3

DO - 10.1016/S0040-4039(01)01113-3

M3 - Article

SN - 0040-4039

VL - 42

SP - 5949

EP - 5951

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 34

ER -

Selenocarbonyl synthesis using Woollins Reagent

Abstract

Keywords

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