Ring size selective synthesis of meso-aryl expanded porphyrins

Ryuichiro Taniguchi; Soji Shimizu; Masaaki Suzuki; Ji Young Shin; Hiroyuki Furuta; Atsuhiro Osuka

doi:10.1016/S0040-4039(03)00328-9

Ring size selective synthesis of meso-aryl expanded porphyrins

Ryuichiro Taniguchi
, Soji Shimizu
, Masaaki Suzuki
, Ji Young Shin
, Hiroyuki Furuta
, Atsuhiro Osuka

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

77 Citations (Scopus)

Abstract

meso-Aryl expanded porphyrins were prepared in a ring size selective manner from methanesulfonic acid-catalyzed reaction of dipyrromethane and tripyrromethane with aryl aldehydes.

Original language	English
Pages (from-to)	2505-2507
Number of pages	3
Journal	Tetrahedron Letters
Volume	44
Issue number	12
DOIs	https://doi.org/10.1016/S0040-4039(03)00328-9
Publication status	Published - Mar 17 2003

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(03)00328-9

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title = "Ring size selective synthesis of meso-aryl expanded porphyrins",

abstract = "meso-Aryl expanded porphyrins were prepared in a ring size selective manner from methanesulfonic acid-catalyzed reaction of dipyrromethane and tripyrromethane with aryl aldehydes.",

author = "Ryuichiro Taniguchi and Soji Shimizu and Masaaki Suzuki and Shin, \{Ji Young\} and Hiroyuki Furuta and Atsuhiro Osuka",

note = "Funding Information: This work was supported by Grant-in Aids for Scientific Research (No. 111233205 and 12440196) from the Ministry of Education, Science, Sports and Culture of Japan and by CREST (Core Research for Evolutional Science and Technology) and PRESTO (Precursory Research for Embryonic Science and Technology) of Japan Science and Technology Corporation (JST).",

year = "2003",

month = mar,

day = "17",

doi = "10.1016/S0040-4039(03)00328-9",

language = "English",

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pages = "2505--2507",

journal = "Tetrahedron Letters",

issn = "0040-4039",

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TY - JOUR

T1 - Ring size selective synthesis of meso-aryl expanded porphyrins

AU - Taniguchi, Ryuichiro

AU - Shimizu, Soji

AU - Suzuki, Masaaki

AU - Shin, Ji Young

AU - Furuta, Hiroyuki

AU - Osuka, Atsuhiro

N1 - Funding Information: This work was supported by Grant-in Aids for Scientific Research (No. 111233205 and 12440196) from the Ministry of Education, Science, Sports and Culture of Japan and by CREST (Core Research for Evolutional Science and Technology) and PRESTO (Precursory Research for Embryonic Science and Technology) of Japan Science and Technology Corporation (JST).

PY - 2003/3/17

Y1 - 2003/3/17

N2 - meso-Aryl expanded porphyrins were prepared in a ring size selective manner from methanesulfonic acid-catalyzed reaction of dipyrromethane and tripyrromethane with aryl aldehydes.

AB - meso-Aryl expanded porphyrins were prepared in a ring size selective manner from methanesulfonic acid-catalyzed reaction of dipyrromethane and tripyrromethane with aryl aldehydes.

UR - https://www.scopus.com/pages/publications/0037450922

UR - https://www.scopus.com/pages/publications/0037450922#tab=citedBy

U2 - 10.1016/S0040-4039(03)00328-9

DO - 10.1016/S0040-4039(03)00328-9

M3 - Article

AN - SCOPUS:0037450922

SN - 0040-4039

VL - 44

SP - 2505

EP - 2507

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 12

ER -

Ring size selective synthesis of meso-aryl expanded porphyrins

Abstract

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