TANDEM RADICAL REACTIONS OF ISONITRILES WITH 2-PYRIDONYL AND OTHER ARYL RADICALS - SCOPE AND LIMITATIONS, AND A FIRST GENERATION SYNTHESIS OF (+ -)-CAMPTOTHECIN/
Dp. Curran et al., TANDEM RADICAL REACTIONS OF ISONITRILES WITH 2-PYRIDONYL AND OTHER ARYL RADICALS - SCOPE AND LIMITATIONS, AND A FIRST GENERATION SYNTHESIS OF (+ -)-CAMPTOTHECIN/, Tetrahedron, 52(35), 1996, pp. 11385-11404
Photolysis of N-propargyl-6-halo-2-pyridones and related aromatic hali
des in the presence of aryl isonitriles provides tetra- and pentacycli
c products in a single step by a sequence of radical addition to the i
sonitrile followed by two cyclizations. The scope and limitations of t
he process are described along with a first generation synthesis of ra
cemic camptothecin. Copyright (C) 1996 Elsevier Science Ltd