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Volumn 19, Issue 20, 2013, Pages 6203-6208

Synthesis of new functionalized calix[n]phyrin macrocycles with varied ring sizes by using a sterically congested dipyrromethane

Author keywords

calixphyrins; fluorine; heterocycles; lactones; macrocycles; porphyrinoids

Indexed keywords

CALIXPHYRINS; HETEROCYCLES; LACTONES; MACROCYCLES; PORPHYRINOIDS;

EID: 84878380950     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201300179     Document Type: Article
Times cited : (13)

References (39)
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    • See reference [5 a], which describes the condensation of 5-mesityldipyrromethane with acetone yielding the corresponding calix[6]phyrin(1.1. 1.1. 1.1), along with higher-order homologues and side-products, and also one example of meso-dialkylated calix[6]phyrin(1.1. 1.1. 1.1) has been isolated as a byproduct:, D. S. Sharada, A. Z. Muresan, K. Muthukumaran, J. S. Lindsey, J. Org. Chem. 2005, 70, 3500-3510.
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    • Synthesis of a doubly N-confused calix[6]phyrin(1. 1.1. 1. 1.1) by random incorporation of tripyrrane into the macrocyclic framework:, D.-H. Won, M. Toganoh, Y. Terada, S. Fukatsu, H. Uno, H. Furuta, Angew. Chem. 2008, 120, 5518-5521
    • (2008) Angew. Chem. , vol.120 , pp. 5518-5521
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    • Porphyrin 7 has previously been mentioned:, see the Supporting Information for full characterization data
    • Porphyrin 7 has previously been mentioned:, T. Balasubramanian, J. S. Lindsey, Tetrahedron 1999, 55, 6771-6784; see the Supporting Information for full characterization data
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    • Extrusion of tert-butyl groups from a porphyrin under acidic conditions has been described in
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.