An Extremely Simple Route to a Prostaglandin Pre-cursor: Hexamethylphosphoric Triamide-Mediated Conjugate Addition of (E)-1-(Phenylthio)oct-2-enyllithium to 4-t-Butoxycyclopent-2-enone and Triphenyltin Chloride-Assisted Reaction of the Enolate with Methyl 7-Iodohept--5-ynoate

Richard K. Haynes; D.E. Lambert; P.A. Schober; S.G. Turner

An Extremely Simple Route to a Prostaglandin Pre-cursor: Hexamethylphosphoric Triamide-Mediated Conjugate Addition of (E)-1-(Phenylthio)oct-2-enyllithium to 4-t-Butoxycyclopent-2-enone and Triphenyltin Chloride-Assisted Reaction of the Enolate with Methyl 7-Iodohept--5-ynoate

Richard K. Haynes, D.E. Lambert, P.A. Schober, S.G. Turner

The Hong Kong University of Science and Technology

Research output: Contribution to journal › Journal Article

Original language	English
Journal	Aust. J. Chem.
Publication status	Published - 1987

Access to Document

https://hdl.handle.net/1783.1/42781

Cite this

Haynes, R. K., Lambert, D. E., Schober, P. A., & Turner, S. G. (1987). An Extremely Simple Route to a Prostaglandin Pre-cursor: Hexamethylphosphoric Triamide-Mediated Conjugate Addition of (E)-1-(Phenylthio)oct-2-enyllithium to 4-t-Butoxycyclopent-2-enone and Triphenyltin Chloride-Assisted Reaction of the Enolate with Methyl 7-Iodohept--5-ynoate. Aust. J. Chem. https://hdl.handle.net/1783.1/42781

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title = "An Extremely Simple Route to a Prostaglandin Pre-cursor: Hexamethylphosphoric Triamide-Mediated Conjugate Addition of (E)-1-(Phenylthio)oct-2-enyllithium to 4-t-Butoxycyclopent-2-enone and Triphenyltin Chloride-Assisted Reaction of the Enolate with Methyl 7-Iodohept--5-ynoate",

author = "Haynes, \{Richard K.\} and D.E. Lambert and P.A. Schober and S.G. Turner",

year = "1987",

language = "English",

journal = "Aust. J. Chem.",

issn = "0004-9425",

publisher = "CSIRO Publishing ",

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Haynes, RK, Lambert, DE, Schober, PA & Turner, SG 1987, 'An Extremely Simple Route to a Prostaglandin Pre-cursor: Hexamethylphosphoric Triamide-Mediated Conjugate Addition of (E)-1-(Phenylthio)oct-2-enyllithium to 4-t-Butoxycyclopent-2-enone and Triphenyltin Chloride-Assisted Reaction of the Enolate with Methyl 7-Iodohept--5-ynoate', Aust. J. Chem. <https://hdl.handle.net/1783.1/42781>

An Extremely Simple Route to a Prostaglandin Pre-cursor: Hexamethylphosphoric Triamide-Mediated Conjugate Addition of (E)-1-(Phenylthio)oct-2-enyllithium to 4-t-Butoxycyclopent-2-enone and Triphenyltin Chloride-Assisted Reaction of the Enolate with Methyl 7-Iodohept--5-ynoate. / Haynes, Richard K.; Lambert, D.E.; Schober, P.A. et al.
In: Aust. J. Chem., 1987.

Research output: Contribution to journal › Journal Article

TY - JOUR

T1 - An Extremely Simple Route to a Prostaglandin Pre-cursor: Hexamethylphosphoric Triamide-Mediated Conjugate Addition of (E)-1-(Phenylthio)oct-2-enyllithium to 4-t-Butoxycyclopent-2-enone and Triphenyltin Chloride-Assisted Reaction of the Enolate with Methyl 7-Iodohept--5-ynoate

AU - Haynes, Richard K.

AU - Lambert, D.E.

AU - Schober, P.A.

AU - Turner, S.G.

PY - 1987

Y1 - 1987

M3 - Journal Article

SN - 0004-9425

JO - Aust. J. Chem.

JF - Aust. J. Chem.

ER -