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The cycloaddition of cyclopropenes to enones

Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid

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The cycloaddition of cyclopropenes to enones. / Al Dulayymi, JR; Baird, MS; Hussain, HH et al.
Yn: Tetrahedron Letters, Cyfrol 41, Rhif 21, 29.05.2000, t. 4205-4208.

Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid

HarvardHarvard

Al Dulayymi, JR, Baird, MS, Hussain, HH, Alhourani, BJ, Alhabashna, AMY, Coles, SJ & Hursthouse, MB 2000, 'The cycloaddition of cyclopropenes to enones', Tetrahedron Letters, cyfrol. 41, rhif 21, tt. 4205-4208. https://doi.org/10.1016/S0040-4039(00)00566-9

APA

Al Dulayymi, JR., Baird, MS., Hussain, HH., Alhourani, BJ., Alhabashna, AMY., Coles, SJ., & Hursthouse, MB. (2000). The cycloaddition of cyclopropenes to enones. Tetrahedron Letters, 41(21), 4205-4208. https://doi.org/10.1016/S0040-4039(00)00566-9

CBE

Al Dulayymi JR, Baird MS, Hussain HH, Alhourani BJ, Alhabashna AMY, Coles SJ, Hursthouse MB. 2000. The cycloaddition of cyclopropenes to enones. Tetrahedron Letters. 41(21):4205-4208. https://doi.org/10.1016/S0040-4039(00)00566-9

MLA

Al Dulayymi, JR et al. "The cycloaddition of cyclopropenes to enones". Tetrahedron Letters. 2000, 41(21). 4205-4208. https://doi.org/10.1016/S0040-4039(00)00566-9

VancouverVancouver

Al Dulayymi JR, Baird MS, Hussain HH, Alhourani BJ, Alhabashna AMY, Coles SJ et al. The cycloaddition of cyclopropenes to enones. Tetrahedron Letters. 2000 Mai 29;41(21):4205-4208. doi: 10.1016/S0040-4039(00)00566-9

Author

Al Dulayymi, JR ; Baird, MS ; Hussain, HH et al. / The cycloaddition of cyclopropenes to enones. Yn: Tetrahedron Letters. 2000 ; Cyfrol 41, Rhif 21. tt. 4205-4208.

RIS

TY - JOUR

T1 - The cycloaddition of cyclopropenes to enones

AU - Al Dulayymi, JR

AU - Baird, MS

AU - Hussain, HH

AU - Alhourani, BJ

AU - Alhabashna, AMY

AU - Coles, SJ

AU - Hursthouse, MB

PY - 2000/5/29

Y1 - 2000/5/29

N2 - A number of 1- and 1,2-disubstituted cyclopropenes undergo [4+2]-cycloaddition to methyl vinyl ketone or acrolein at ambient temperature to produce 2-oxabicyclo[4.1.0]hept-3-enes. When 1-phenyl-2-trimethylsilyl cyclopropene is treated with 0.4 mel. equiv. of m-chloroperbenzoic acid, the derived ring-opened enone undergoes [4+2]-cycloaddition to the remaining starting material at ambient temperature. (C) 2000 Elsevier Science Ltd. All rights reserved.

AB - A number of 1- and 1,2-disubstituted cyclopropenes undergo [4+2]-cycloaddition to methyl vinyl ketone or acrolein at ambient temperature to produce 2-oxabicyclo[4.1.0]hept-3-enes. When 1-phenyl-2-trimethylsilyl cyclopropene is treated with 0.4 mel. equiv. of m-chloroperbenzoic acid, the derived ring-opened enone undergoes [4+2]-cycloaddition to the remaining starting material at ambient temperature. (C) 2000 Elsevier Science Ltd. All rights reserved.

U2 - 10.1016/S0040-4039(00)00566-9

DO - 10.1016/S0040-4039(00)00566-9

M3 - Article

VL - 41

SP - 4205

EP - 4208

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 21

ER -