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Asymmetric aziridine synthesis via aza-Darzens reaction of bromoacylcamphorsultam

Research output: Contribution to Journal/Magazine › Journal article › peer-review

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Asymmetric aziridine synthesis via aza-Darzens reaction of bromoacylcamphorsultam. / Cantrill, Alex A.; Hall, Lee D.; Jarvis, Ashley N. et al.
In: Chemical Communications, Vol. 1996, No. 23, 01.01.1996, p. 2631-2632.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Cantrill, AA, Hall, LD, Jarvis, AN, Osborn, HMI, Raphy, J & Sweeney, JB 1996, 'Asymmetric aziridine synthesis via aza-Darzens reaction of bromoacylcamphorsultam', Chemical Communications, vol. 1996, no. 23, pp. 2631-2632. https://doi.org/10.1039/cc9960002631

APA

Cantrill, A. A., Hall, L. D., Jarvis, A. N., Osborn, H. M. I., Raphy, J., & Sweeney, J. B. (1996). Asymmetric aziridine synthesis via aza-Darzens reaction of bromoacylcamphorsultam. Chemical Communications, 1996(23), 2631-2632. https://doi.org/10.1039/cc9960002631

Vancouver

Cantrill AA, Hall LD, Jarvis AN, Osborn HMI, Raphy J, Sweeney JB. Asymmetric aziridine synthesis via aza-Darzens reaction of bromoacylcamphorsultam. Chemical Communications. 1996 Jan 1;1996(23):2631-2632. doi: 10.1039/cc9960002631

Author

Cantrill, Alex A. ; Hall, Lee D. ; Jarvis, Ashley N. et al. / Asymmetric aziridine synthesis via aza-Darzens reaction of bromoacylcamphorsultam. In: Chemical Communications. 1996 ; Vol. 1996, No. 23. pp. 2631-2632.

Bibtex

@article{cd54ddb23d9448b3b93580b27fdb7e5c,
title = "Asymmetric aziridine synthesis via aza-Darzens reaction of bromoacylcamphorsultam",
abstract = "The aza-Darzens reaction of the chiral enolate derived from bromoacetylcamphorsultam 1 with N-(diphenylphosphinyl)aryl- and tert-butyl-methanimines proceeds in good yield to give cis-N-(diphenylphosphinyl)aziridinylcarbonyl sultams with high de. Monochiral cis-aziridinecarboxylates may be obtained in acceptable yield by hydrolysis of these sultams.",
author = "Cantrill, {Alex A.} and Hall, {Lee D.} and Jarvis, {Ashley N.} and Osborn, {Helen M.I.} and Jenny Raphy and Sweeney, {J. B.}",
year = "1996",
month = jan,
day = "1",
doi = "10.1039/cc9960002631",
language = "English",
volume = "1996",
pages = "2631--2632",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "23",

}

RIS

TY - JOUR

T1 - Asymmetric aziridine synthesis via aza-Darzens reaction of bromoacylcamphorsultam

AU - Cantrill, Alex A.

AU - Hall, Lee D.

AU - Jarvis, Ashley N.

AU - Osborn, Helen M.I.

AU - Raphy, Jenny

AU - Sweeney, J. B.

PY - 1996/1/1

Y1 - 1996/1/1

N2 - The aza-Darzens reaction of the chiral enolate derived from bromoacetylcamphorsultam 1 with N-(diphenylphosphinyl)aryl- and tert-butyl-methanimines proceeds in good yield to give cis-N-(diphenylphosphinyl)aziridinylcarbonyl sultams with high de. Monochiral cis-aziridinecarboxylates may be obtained in acceptable yield by hydrolysis of these sultams.

AB - The aza-Darzens reaction of the chiral enolate derived from bromoacetylcamphorsultam 1 with N-(diphenylphosphinyl)aryl- and tert-butyl-methanimines proceeds in good yield to give cis-N-(diphenylphosphinyl)aziridinylcarbonyl sultams with high de. Monochiral cis-aziridinecarboxylates may be obtained in acceptable yield by hydrolysis of these sultams.

U2 - 10.1039/cc9960002631

DO - 10.1039/cc9960002631

M3 - Journal article

AN - SCOPUS:0001932039

VL - 1996

SP - 2631

EP - 2632

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 23

ER -