Utilization of a nitrenium ion cyclization in a synthesis of a photoactive prostaglandin, 17-(4-azido-2-hydroxyphenyl)-18,19,20-trinorprostaglandin F2/ga

E. Kurt Dolence; Hiroyuki Morita; David S. Watt; Tony Fitz

doi:10.1016/S0040-4039(00)95644-2

Utilization of a nitrenium ion cyclization in a synthesis of a photoactive prostaglandin, 17-(4-azido-2-hydroxyphenyl)-18,19,20-trinorprostaglandin F₂/ga

E. Kurt Dolence
, Hiroyuki Morita
, David S. Watt
, Tony Fitz

Molecular and Cellular Biochemistry

Producción científica: Article › revisión exhaustiva

7 Citas (Scopus)

Resumen

A nitrenium ion cyclization provided access to a suitably substituted arylpropionic ester needed in the synthesis of a potential prostaglandin photoaffinity probe, 17-(4-azido-2-hydroxyphenyl)-18,19,20-trinorprostaglandin F₂α using the Corey synthesis.

Idioma original	English
Páginas (desde-hasta)	43-46
Número de páginas	4
Publicación	Tetrahedron Letters
Volumen	28
N.º	1
DOI	https://doi.org/10.1016/S0040-4039(00)95644-2
Estado	Published - 1987

Nota bibliográfica

Funding Information:
Acknowledgement. We thank the National Institutes generous financial support, the Upjohn Company for the Midwest Center for Mass Spectrometry for exact of Health (HL 20780) for a gift of chemicals, and mass spectra.

Financiación

Acknowledgement. We thank the National Institutes generous financial support, the Upjohn Company for the Midwest Center for Mass Spectrometry for exact of Health (HL 20780) for a gift of chemicals, and mass spectra.

Financiadores	Número del financiador
National Institutes of Health (NIH)
Upjohn Company for the Midwest Center for Mass Spectrometry for exact of Health	HL 20780

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)95644-2

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abstract = "A nitrenium ion cyclization provided access to a suitably substituted arylpropionic ester needed in the synthesis of a potential prostaglandin photoaffinity probe, 17-(4-azido-2-hydroxyphenyl)-18,19,20-trinorprostaglandin F2α using the Corey synthesis.",

author = "Dolence, \{E. Kurt\} and Hiroyuki Morita and Watt, \{David S.\} and Tony Fitz",

note = "Funding Information: Acknowledgement. We thank the National Institutes generous financial support, the Upjohn Company for the Midwest Center for Mass Spectrometry for exact of Health (HL 20780) for a gift of chemicals, and mass spectra.",

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doi = "10.1016/S0040-4039(00)95644-2",

language = "English",

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AU - Dolence, E. Kurt

AU - Morita, Hiroyuki

AU - Watt, David S.

AU - Fitz, Tony

N1 - Funding Information: Acknowledgement. We thank the National Institutes generous financial support, the Upjohn Company for the Midwest Center for Mass Spectrometry for exact of Health (HL 20780) for a gift of chemicals, and mass spectra.

PY - 1987

Y1 - 1987

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AB - A nitrenium ion cyclization provided access to a suitably substituted arylpropionic ester needed in the synthesis of a potential prostaglandin photoaffinity probe, 17-(4-azido-2-hydroxyphenyl)-18,19,20-trinorprostaglandin F2α using the Corey synthesis.

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DO - 10.1016/S0040-4039(00)95644-2

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