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Tributyltin hydride-mediated tandem reactions of dehydroalanines leading to alpha-substituted pyroglutamates

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Tributyltin hydride-mediated tandem reactions of dehydroalanines leading to alpha-substituted pyroglutamates. / Baker, S R ; Goodall, K ; Parsons, A F ; Wilson, M .

In: JOURNAL OF CHEMICAL RESEARCH-S, No. 7, 07.2000, p. 312-313.

Research output: Contribution to journalArticle

Harvard

Baker, SR, Goodall, K, Parsons, AF & Wilson, M 2000, 'Tributyltin hydride-mediated tandem reactions of dehydroalanines leading to alpha-substituted pyroglutamates', JOURNAL OF CHEMICAL RESEARCH-S, no. 7, pp. 312-313.

APA

Baker, S. R., Goodall, K., Parsons, A. F., & Wilson, M. (2000). Tributyltin hydride-mediated tandem reactions of dehydroalanines leading to alpha-substituted pyroglutamates. JOURNAL OF CHEMICAL RESEARCH-S, (7), 312-313.

Vancouver

Baker SR, Goodall K, Parsons AF, Wilson M. Tributyltin hydride-mediated tandem reactions of dehydroalanines leading to alpha-substituted pyroglutamates. JOURNAL OF CHEMICAL RESEARCH-S. 2000 Jul;(7):312-313.

Author

Baker, S R ; Goodall, K ; Parsons, A F ; Wilson, M . / Tributyltin hydride-mediated tandem reactions of dehydroalanines leading to alpha-substituted pyroglutamates. In: JOURNAL OF CHEMICAL RESEARCH-S. 2000 ; No. 7. pp. 312-313.

Bibtex - Download

@article{2b77f26facb147caac7653d3fa2cb918,
title = "Tributyltin hydride-mediated tandem reactions of dehydroalanines leading to alpha-substituted pyroglutamates",
abstract = "Tributyltin hydride-mediated cyclisation of dehydroalanines produces an intermediate captodative radical, which can be trapped by reaction with oxygen- or carbon-centred radicals or (principally) electron-poor alkenes, to provide a quick approach to a variety of alpha-substituted pyroglutamates.",
keywords = "RADICAL CYCLIZATION, SECONDARY AMIDES, PYRROLIDINONES, 5-ENDO-TRIG, 4-EXO-TRIG",
author = "Baker, {S R} and K Goodall and Parsons, {A F} and M Wilson",
year = "2000",
month = jul,
language = "English",
pages = "312--313",
journal = "JOURNAL OF CHEMICAL RESEARCH-S",
issn = "0308-2342",
publisher = "Science Reviews Ltd",
number = "7",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - Tributyltin hydride-mediated tandem reactions of dehydroalanines leading to alpha-substituted pyroglutamates

AU - Baker, S R

AU - Goodall, K

AU - Parsons, A F

AU - Wilson, M

PY - 2000/7

Y1 - 2000/7

N2 - Tributyltin hydride-mediated cyclisation of dehydroalanines produces an intermediate captodative radical, which can be trapped by reaction with oxygen- or carbon-centred radicals or (principally) electron-poor alkenes, to provide a quick approach to a variety of alpha-substituted pyroglutamates.

AB - Tributyltin hydride-mediated cyclisation of dehydroalanines produces an intermediate captodative radical, which can be trapped by reaction with oxygen- or carbon-centred radicals or (principally) electron-poor alkenes, to provide a quick approach to a variety of alpha-substituted pyroglutamates.

KW - RADICAL CYCLIZATION

KW - SECONDARY AMIDES

KW - PYRROLIDINONES

KW - 5-ENDO-TRIG

KW - 4-EXO-TRIG

M3 - Article

SP - 312

EP - 313

JO - JOURNAL OF CHEMICAL RESEARCH-S

JF - JOURNAL OF CHEMICAL RESEARCH-S

SN - 0308-2342

IS - 7

ER -