The synthesis and attempted ring closure of ethyl 3-(aminomethyl)-7,8,12,13,17,18-hexaethylporphyrin-2-carboxylate

Roger F C Brown; Patrick Perlmutter; Helen K Tope

doi:10.1071/CH9951447

The synthesis and attempted ring closure of ethyl 3-(aminomethyl)-7,8,12,13,17,18-hexaethylporphyrin-2-carboxylate

Roger F C Brown, Patrick Perlmutter, Helen K Tope

School of Chemistry

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

3 Citations (Scopus)

Abstract

A synthesis of the porphyrin amino ester deriv. I is described. All attempts to convert I into a fused pyrroloporphyrin were unsuccessful, with the corresponding 2-formylporphyrin being formed instead. [on SciFinder(R)]

Original language	English
Pages (from-to)	1447 - 1452
Number of pages	6
Journal	Australian Journal of Chemistry
Volume	48
Issue number	8
DOIs	https://doi.org/10.1071/CH9951447
Publication status	Published - 1995

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@article{a589a1cef4704c85aa99d28da557c2a5,

title = "The synthesis and attempted ring closure of ethyl 3-(aminomethyl)-7,8,12,13,17,18-hexaethylporphyrin-2-carboxylate",

abstract = "A synthesis of the porphyrin amino ester deriv. I is described. All attempts to convert I into a fused pyrroloporphyrin were unsuccessful, with the corresponding 2-formylporphyrin being formed instead. [on SciFinder(R)]",

author = "Brown, {Roger F C} and Patrick Perlmutter and Tope, {Helen K}",

year = "1995",

doi = "10.1071/CH9951447",

language = "English",

volume = "48",

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journal = "Australian Journal of Chemistry",

issn = "0004-9425",

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T1 - The synthesis and attempted ring closure of ethyl 3-(aminomethyl)-7,8,12,13,17,18-hexaethylporphyrin-2-carboxylate

AU - Brown, Roger F C

AU - Perlmutter, Patrick

AU - Tope, Helen K

PY - 1995

Y1 - 1995

N2 - A synthesis of the porphyrin amino ester deriv. I is described. All attempts to convert I into a fused pyrroloporphyrin were unsuccessful, with the corresponding 2-formylporphyrin being formed instead. [on SciFinder(R)]

AB - A synthesis of the porphyrin amino ester deriv. I is described. All attempts to convert I into a fused pyrroloporphyrin were unsuccessful, with the corresponding 2-formylporphyrin being formed instead. [on SciFinder(R)]

UR - http://www.publish.csiro.au/?act=view_file&file_id=CH9951447.pdf

U2 - 10.1071/CH9951447

DO - 10.1071/CH9951447

M3 - Article

VL - 48

SP - 1447

EP - 1452

JO - Australian Journal of Chemistry

JF - Australian Journal of Chemistry

SN - 0004-9425

IS - 8

ER -

The synthesis and attempted ring closure of ethyl 3-(aminomethyl)-7,8,12,13,17,18-hexaethylporphyrin-2-carboxylate

Abstract

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