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Cyclisation of dienes using phosphorus-centred radicals to form organophosphorus adducts

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Cyclisation of dienes using phosphorus-centred radicals to form organophosphorus adducts. / Jessop, C M ; Parsons, A F ; Routledge, A ; Irvine, D .

In: Tetrahedron Letters, Vol. 44, No. 3, 13.01.2003, p. 479-483.

Research output: Contribution to journalArticle

Harvard

Jessop, CM, Parsons, AF, Routledge, A & Irvine, D 2003, 'Cyclisation of dienes using phosphorus-centred radicals to form organophosphorus adducts', Tetrahedron Letters, vol. 44, no. 3, pp. 479-483.

APA

Jessop, C. M., Parsons, A. F., Routledge, A., & Irvine, D. (2003). Cyclisation of dienes using phosphorus-centred radicals to form organophosphorus adducts. Tetrahedron Letters, 44(3), 479-483.

Vancouver

Jessop CM, Parsons AF, Routledge A, Irvine D. Cyclisation of dienes using phosphorus-centred radicals to form organophosphorus adducts. Tetrahedron Letters. 2003 Jan 13;44(3):479-483.

Author

Jessop, C M ; Parsons, A F ; Routledge, A ; Irvine, D . / Cyclisation of dienes using phosphorus-centred radicals to form organophosphorus adducts. In: Tetrahedron Letters. 2003 ; Vol. 44, No. 3. pp. 479-483.

Bibtex - Download

@article{f2b65903ae0b4d2caee5a2ad91daadc6,
title = "Cyclisation of dienes using phosphorus-centred radicals to form organophosphorus adducts",
abstract = "Reaction of various dienes with phosphites or related phosphorus hydrides, under free radical cyclisation conditions, affords cyclic organophosphorus adducts. This quick, mild and technically clean approach affords 5- and 6-ring carbocycles and heterocycles in good to excellent yield. (C) 2002 Elsevier Science Ltd. All rights reserved.",
keywords = "cyclisation, dienes, phosphorus compounds, radicals and radical reactions, CYCLIZATION REACTIONS, TRIBUTYLTIN HYDRIDE, PHOSPHINIC ACID, EFFICIENT, HETEROCYCLES, GENERATION, ALKENES, PHOSPHONOTHIOATES, REARRANGEMENT, HYPOPHOSPHITE",
author = "Jessop, {C M} and Parsons, {A F} and A Routledge and D Irvine",
year = "2003",
month = "1",
day = "13",
language = "English",
volume = "44",
pages = "479--483",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "3",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - Cyclisation of dienes using phosphorus-centred radicals to form organophosphorus adducts

AU - Jessop, C M

AU - Parsons, A F

AU - Routledge, A

AU - Irvine, D

PY - 2003/1/13

Y1 - 2003/1/13

N2 - Reaction of various dienes with phosphites or related phosphorus hydrides, under free radical cyclisation conditions, affords cyclic organophosphorus adducts. This quick, mild and technically clean approach affords 5- and 6-ring carbocycles and heterocycles in good to excellent yield. (C) 2002 Elsevier Science Ltd. All rights reserved.

AB - Reaction of various dienes with phosphites or related phosphorus hydrides, under free radical cyclisation conditions, affords cyclic organophosphorus adducts. This quick, mild and technically clean approach affords 5- and 6-ring carbocycles and heterocycles in good to excellent yield. (C) 2002 Elsevier Science Ltd. All rights reserved.

KW - cyclisation

KW - dienes

KW - phosphorus compounds

KW - radicals and radical reactions

KW - CYCLIZATION REACTIONS

KW - TRIBUTYLTIN HYDRIDE

KW - PHOSPHINIC ACID

KW - EFFICIENT

KW - HETEROCYCLES

KW - GENERATION

KW - ALKENES

KW - PHOSPHONOTHIOATES

KW - REARRANGEMENT

KW - HYPOPHOSPHITE

M3 - Article

VL - 44

SP - 479

EP - 483

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 3

ER -