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Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes

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

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Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes. / Baldwin, Jack E.; Adlington, Robert M.; Lowe, Christopher et al.

In: Journal of the Chemical Society, Chemical Communications, No. 15, 01.01.1988, p. 1030-1031.

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

Harvard

Baldwin, JE, Adlington, RM, Lowe, C, O'Neil, IA, Sanders, GL, Schofield, CJ & Sweeney, JB 1988, 'Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes', Journal of the Chemical Society, Chemical Communications, no. 15, pp. 1030-1031. https://doi.org/10.1039/C39880001030

APA

Baldwin, J. E., Adlington, R. M., Lowe, C., O'Neil, I. A., Sanders, G. L., Schofield, C. J., & Sweeney, J. B. (1988). Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes. Journal of the Chemical Society, Chemical Communications, (15), 1030-1031. https://doi.org/10.1039/C39880001030

Vancouver

Baldwin JE, Adlington RM, Lowe C, O'Neil IA, Sanders GL, Schofield CJ et al. Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes. Journal of the Chemical Society, Chemical Communications. 1988 Jan 1;(15):1030-1031. doi: 10.1039/C39880001030

Author

Baldwin, Jack E. ; Adlington, Robert M. ; Lowe, Christopher et al. / Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes. In: Journal of the Chemical Society, Chemical Communications. 1988 ; No. 15. pp. 1030-1031.

Bibtex

@article{27ca4d3e48404193a076de04cf0d69b0,
title = "Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes",
abstract = "Reaction of 2-bromo-N-benzoylglycine methyl ester with 2-functionalised allyl stannane reagents under radical conditions provides a new route to α-alkylated amino acids in good yield, as exemplified by the facile synthesis of 4-methylene glutamate.",
author = "Baldwin, {Jack E.} and Adlington, {Robert M.} and Christopher Lowe and O'Neil, {Ian A.} and Sanders, {Gillian L.} and Schofield, {Christopher J.} and Sweeney, {Joseph B.}",
year = "1988",
month = jan,
day = "1",
doi = "10.1039/C39880001030",
language = "English",
pages = "1030--1031",
journal = "Journal of the Chemical Society, Chemical Communications",
issn = "0022-4936",
publisher = "Chemical Society",
number = "15",

}

RIS

TY - JOUR

T1 - Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes

AU - Baldwin, Jack E.

AU - Adlington, Robert M.

AU - Lowe, Christopher

AU - O'Neil, Ian A.

AU - Sanders, Gillian L.

AU - Schofield, Christopher J.

AU - Sweeney, Joseph B.

PY - 1988/1/1

Y1 - 1988/1/1

N2 - Reaction of 2-bromo-N-benzoylglycine methyl ester with 2-functionalised allyl stannane reagents under radical conditions provides a new route to α-alkylated amino acids in good yield, as exemplified by the facile synthesis of 4-methylene glutamate.

AB - Reaction of 2-bromo-N-benzoylglycine methyl ester with 2-functionalised allyl stannane reagents under radical conditions provides a new route to α-alkylated amino acids in good yield, as exemplified by the facile synthesis of 4-methylene glutamate.

U2 - 10.1039/C39880001030

DO - 10.1039/C39880001030

M3 - Journal article

AN - SCOPUS:37049069728

SP - 1030

EP - 1031

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

SN - 0022-4936

IS - 15

ER -