Abstract
The first representative of a new class of porphyrins featuring a tetramethine bridge joining the 2 and 20 positions of the macrocycle has been prepared and found to undergo the Diels-Alder reaction, yielding structures in which functional groups are linked to the porphyrin macrocycle through a rigid, bicyclic bridge.
Original language | English (US) |
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Pages (from-to) | 995-998 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 35 |
Issue number | 7 |
DOIs | |
State | Published - Feb 14 1994 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry