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Fukui, Norihito, Yorimitsu, Hideki, Osuka, Atsuhiro (2015) meso,β-Oligohaloporphyrins as Useful Synthetic Intermediates of Diphenylamine-Fused Porphyrin and meso-to-meso β-to-β Doubly Butadiyne-Bridged Diporphyrin. Angewandte Chemie, 127 (21). 6409-6412 doi:10.1002/ange.201501149

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Reference TypeJournal (article/letter/editorial)
Titlemeso,β-Oligohaloporphyrins as Useful Synthetic Intermediates of Diphenylamine-Fused Porphyrin and meso-to-meso β-to-β Doubly Butadiyne-Bridged Diporphyrin
JournalAngewandte Chemie
AuthorsFukui, NorihitoAuthor
Yorimitsu, HidekiAuthor
Osuka, AtsuhiroAuthor
Year2015 (May 18)Volume127
Issue21
PublisherWiley
DOIdoi:10.1002/ange.201501149Search in ResearchGate
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Mindat Ref. ID7328204Long-form Identifiermindat:1:5:7328204:6
GUID0
Full ReferenceFukui, Norihito, Yorimitsu, Hideki, Osuka, Atsuhiro (2015) meso,β-Oligohaloporphyrins as Useful Synthetic Intermediates of Diphenylamine-Fused Porphyrin and meso-to-meso β-to-β Doubly Butadiyne-Bridged Diporphyrin. Angewandte Chemie, 127 (21). 6409-6412 doi:10.1002/ange.201501149
Plain TextFukui, Norihito, Yorimitsu, Hideki, Osuka, Atsuhiro (2015) meso,β-Oligohaloporphyrins as Useful Synthetic Intermediates of Diphenylamine-Fused Porphyrin and meso-to-meso β-to-β Doubly Butadiyne-Bridged Diporphyrin. Angewandte Chemie, 127 (21). 6409-6412 doi:10.1002/ange.201501149
In(2015, May) Angewandte Chemie Vol. 127 (21) Wiley

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Fukui, Norihito, Yorimitsu, Hideki, Osuka, Atsuhiro (2015) meso,β-Oligohaloporphyrins as Useful Synthetic Intermediates of Diphenylamine-Fused Porphyrin and meso-to-meso β-to-β Doubly Butadiyne-Bridged Diporphyrin. Angewandte Chemie International Edition, 54 (21). 6311-6314 doi:10.1002/anie.201501149
Fukui, Norihito, Yorimitsu, Hideki, Osuka, Atsuhiro (2016) meso-meso-Linked Diarylamine-Fused Porphyrin Dimers. Chemistry - A European Journal, 22 (51). 18476-18483 doi:10.1002/chem.201604301
Fukui, Norihito, Yorimitsu, Hideki, Lim, Jong Min, Kim, Dongho, Osuka, Atsuhiro (2014) Synthesis of 7,8-Dehydropurpurin Dimers and Their Conversion into Conformationally Constrained β-to-β Vinylene-Bridged Porphyrin Dimers. Angewandte Chemie, 126 (17). 4484-4487 doi:10.1002/ange.201400632
Tanaka, Yasuo, Mori, Hirotaka, Koide, Taro, Yorimitsu, Hideki, Aratani, Naoki, Osuka, Atsuhiro (2011) Rearrangements of a [36]Octaphyrin Triggered by Nickel(II) Metalation: Metamorphosis to a Directly meso-β-Linked Diporphyrin. Angewandte Chemie, 123 (48). 11662-11666 doi:10.1002/ange.201105809
Kitano, Masaaki, Okuda, Yasuhiro, Tsurumaki, Eiji, Tanaka, Takayuki, Yorimitsu, Hideki, Osuka, Atsuhiro (2015) β,β-Diborylated Subporphyrinato Boron(III) Complexes as Useful Synthetic Precursors. Angewandte Chemie, 127 (32). 9407-9411 doi:10.1002/ange.201503530
Fukui, Norihito, Yorimitsu, Hideki, Lim, Jong Min, Kim, Dongho, Osuka, Atsuhiro (2014) Synthesis of 7,8-Dehydropurpurin Dimers and Their Conversion into Conformationally Constrained β-to-β Vinylene-Bridged Porphyrin Dimers. Angewandte Chemie International Edition, 53 (17). 4395-4398 doi:10.1002/anie.201400632
Song, Jianxin, Aratani, Naoki, Kim, Pyosang, Kim, Dongho, Shinokubo, Hiroshi, Osuka, Atsuhiro (2010) Porphyrin “Lego Block” Strategy To Construct Directly meso-β Doubly Linked Porphyrin Rings. Angewandte Chemie, 122 (21). 3699-3702 doi:10.1002/ange.201000915
Tanaka, Yasuo, Mori, Hirotaka, Koide, Taro, Yorimitsu, Hideki, Aratani, Naoki, Osuka, Atsuhiro (2011) Rearrangements of a [36]Octaphyrin Triggered by Nickel(II) Metalation: Metamorphosis to a Directly meso-β-Linked Diporphyrin. Angewandte Chemie International Edition, 50 (48). 11460-11464 doi:10.1002/anie.201105809
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Song, Jianxin, Aratani, Naoki, Kim, Pyosang, Kim, Dongho, Shinokubo, Hiroshi, Osuka, Atsuhiro (2010) Porphyrin “Lego Block” Strategy To Construct Directly meso-β Doubly Linked Porphyrin Rings. Angewandte Chemie International Edition, 49 (21). 3617-3620 doi:10.1002/anie.201000915
Kitano, Masaaki, Okuda, Yasuhiro, Tsurumaki, Eiji, Tanaka, Takayuki, Yorimitsu, Hideki, Osuka, Atsuhiro (2015) β,β-Diborylated Subporphyrinato Boron(III) Complexes as Useful Synthetic Precursors. Angewandte Chemie International Edition, 54 (32). 9275-9279 doi:10.1002/anie.201503530
 
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