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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doi = "10.1016/S0040-4039(00)01899-2",

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T1 - A concise efficient route to fumitromorgins

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

Y1 - 2001/1/1

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.

KW - Alkaloids

KW - Anti-tumour

KW - Indoles

KW - Pictet-Spengler

UR - https://www.scopus.com/pages/publications/0035185881

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

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

M3 - Article

SN - 0040-4039

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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