Reaction of purpurins (1a,b) with DDQ resulted in oxidative ring closu
re at ring D to give novel delta-lactones (2a,b), mild treatment of wh
ich with TFA/methanol gave chlorins (3a,b) possessing a hydroxy group
at C-18. Prolonged treatment of (3a,b) with TFA resulted in their dehy
dration and the formation of porphyrins (4a,b). (C) 1997 Elsevier Scie
nce Ltd.