Highly efficient synthesis of extended triptycenes via Diels-Alder cycloaddition in water under microwave radiation

Tetrahedron Letters

Volumn 51, Issue 34, 2010, Pages 4519-4522

  Pei, Bao Jian ^a   Lee, Albert W M ^a  

^a HONG KONG BAPTIST UNIVERSITY   (Hong Kong)

Author keywords

Dehydration; Diels Alder cycloaddition; Endoxides; Extended triptycene; Microwave

Indexed keywords

ACETIC ANHYDRIDE; ACETYL HYDROXIDE; HYDROXIDE; TRIPTYCENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CYCLOADDITION; DIELS ALDER REACTION; MICROWAVE RADIATION; SYNTHESIS;

ALNUS;

EID: 77955714427     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.06.097     Document Type: Article

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47. 3): δ = 47.5, 49.0, 53.6, 81.2, 116.6, 122.0, 123.5, 123.6, 123.7, 125.3, 125.4, 125.7, 126.0, 130.7, 141.4, 142.1, 144.0, 144.4, 144.5, 144.6.
48. 3): δ = 1.2, 1.3, 109.0, 120.8, 124.7, 124.8, 126.5, 130.9, 134.8, 142.8, 144.2, 151.8.
49. 3): δ = 53.6, 121.3, 123.8, 125.0, 125.6, 130.4, 140.6, 144.2.