A biomimetic synthesis of calothrixin B

Jonathan Sperry; Christopher S. P. McErlean; Alexandra M. Z. Slawin; Christopher J. Moody

doi:10.1016/j.tetlet.2006.11.053

A biomimetic synthesis of calothrixin B

Jonathan Sperry, Christopher S. P. McErlean, Alexandra M. Z. Slawin, Christopher J. Moody

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

Abstract

Oxidation of the indolo[2,3-a]carbazole 15, readily obtained in six steps from indigo, followed by deprotection results in formation of the indolo[3,2-j]phenanthridine quinone alkaloid calothrixin B 2, demonstrating the viability of the proposed biosynthetic route to this unique ring system. (c) 2006 Elsevier Ltd. All rights reserved.

Original language	English
Pages (from-to)	231-234
Number of pages	4
Journal	Tetrahedron Letters
Volume	48
DOIs	https://doi.org/10.1016/j.tetlet.2006.11.053
Publication status	Published - 8 Jan 2007

Keywords

ANTITUMOR AGENTS
OXIDOREDUCTASE
CYANOBACTERIA
METABOLITES
ROUTE

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10.1016/j.tetlet.2006.11.053

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title = "A biomimetic synthesis of calothrixin B",

abstract = "Oxidation of the indolo[2,3-a]carbazole 15, readily obtained in six steps from indigo, followed by deprotection results in formation of the indolo[3,2-j]phenanthridine quinone alkaloid calothrixin B 2, demonstrating the viability of the proposed biosynthetic route to this unique ring system. (c) 2006 Elsevier Ltd. All rights reserved.",

keywords = "ANTITUMOR AGENTS, OXIDOREDUCTASE, CYANOBACTERIA, METABOLITES, ROUTE",

author = "Jonathan Sperry and McErlean, \{Christopher S. P.\} and Slawin, \{Alexandra M. Z.\} and Moody, \{Christopher J.\}",

year = "2007",

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day = "8",

doi = "10.1016/j.tetlet.2006.11.053",

language = "English",

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pages = "231--234",

journal = "Tetrahedron Letters",

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publisher = "Elsevier",

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T1 - A biomimetic synthesis of calothrixin B

AU - Sperry, Jonathan

AU - McErlean, Christopher S. P.

AU - Slawin, Alexandra M. Z.

AU - Moody, Christopher J.

PY - 2007/1/8

Y1 - 2007/1/8

N2 - Oxidation of the indolo[2,3-a]carbazole 15, readily obtained in six steps from indigo, followed by deprotection results in formation of the indolo[3,2-j]phenanthridine quinone alkaloid calothrixin B 2, demonstrating the viability of the proposed biosynthetic route to this unique ring system. (c) 2006 Elsevier Ltd. All rights reserved.

AB - Oxidation of the indolo[2,3-a]carbazole 15, readily obtained in six steps from indigo, followed by deprotection results in formation of the indolo[3,2-j]phenanthridine quinone alkaloid calothrixin B 2, demonstrating the viability of the proposed biosynthetic route to this unique ring system. (c) 2006 Elsevier Ltd. All rights reserved.

KW - ANTITUMOR AGENTS

KW - OXIDOREDUCTASE

KW - CYANOBACTERIA

KW - METABOLITES

KW - ROUTE

UR - https://www.scopus.com/pages/publications/33845232238

U2 - 10.1016/j.tetlet.2006.11.053

DO - 10.1016/j.tetlet.2006.11.053

M3 - Article

SN - 0040-4039

VL - 48

SP - 231

EP - 234

JO - Tetrahedron Letters

JF - Tetrahedron Letters

ER -

A biomimetic synthesis of calothrixin B

Abstract

Keywords

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