A concise efficient route to fumitromorgins

Patrick D. Bailey; Philip J. Cochrane; Katrin Lorenz; Ian D. Collier; D. P J Pearson; Georgina M. Rosair

doi:10.1016/S0040-4039(00)01899-2

A concise efficient route to fumitromorgins

Patrick D. Bailey, Philip J. Cochrane, Katrin Lorenz, Ian D. Collier, D. P J Pearson, Georgina M. Rosair

School of Engineering & Physical Sciences

Research output: Contribution to journal › Article › peer-review

30 Citations (Scopus)

Abstract

Using the kinetically controlled Pictet-Spengler reaction, we have developed a three-step, diastereoselective and enantiospecific synthesis of the natural product demethoxy-fumitremorgin C in 21% overall yield. © 2000 Elsevier Science Ltd.

Original language	English
Pages (from-to)	113-115
Number of pages	3
Journal	Tetrahedron Letters
Volume	42
Issue number	1
DOIs	https://doi.org/10.1016/S0040-4039(00)01899-2
Publication status	Published - 1 Jan 2001

Keywords

Alkaloids
Anti-tumour
Indoles
Pictet-Spengler

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10.1016/S0040-4039(00)01899-2

Cite this

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title = "A concise efficient route to fumitromorgins",

abstract = "Using the kinetically controlled Pictet-Spengler reaction, we have developed a three-step, diastereoselective and enantiospecific synthesis of the natural product demethoxy-fumitremorgin C in 21% overall yield. {\textcopyright} 2000 Elsevier Science Ltd.",

keywords = "Alkaloids, Anti-tumour, Indoles, Pictet-Spengler",

author = "Bailey, {Patrick D.} and Cochrane, {Philip J.} and Katrin Lorenz and Collier, {Ian D.} and Pearson, {D. P J} and Rosair, {Georgina M.}",

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AU - Bailey, Patrick D.

AU - Cochrane, Philip J.

AU - Lorenz, Katrin

AU - Collier, Ian D.

AU - Pearson, D. P J

AU - Rosair, Georgina M.

PY - 2001/1/1

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N2 - Using the kinetically controlled Pictet-Spengler reaction, we have developed a three-step, diastereoselective and enantiospecific synthesis of the natural product demethoxy-fumitremorgin C in 21% overall yield. © 2000 Elsevier Science Ltd.

AB - Using the kinetically controlled Pictet-Spengler reaction, we have developed a three-step, diastereoselective and enantiospecific synthesis of the natural product demethoxy-fumitremorgin C in 21% overall yield. © 2000 Elsevier Science Ltd.

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KW - Anti-tumour

KW - Indoles

KW - Pictet-Spengler

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U2 - 10.1016/S0040-4039(00)01899-2

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VL - 42

SP - 113

EP - 115

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 1

ER -

A concise efficient route to fumitromorgins

Abstract

Keywords

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