A Heat and Light Mediated Synthetic Sequence Serendipitous Synthesis of Methyl Ester of Tris-Norpterosin-E

References

• de Mayo , P. , ed. 1980 . Vol 1–3 , New York : Academic press . Rearrangements in the ground and excited states
   Google Scholar
• Mehta , G. , Srikrishna , A. and Suri , S. C. 1980 . J. Org. Cham. , 45 : 5375 Mehta, G. and Nair, M.S., J. Am. Chem. Soc., 1985, 107, 7519; Mehta, G. and Reddy, K.R., Tetrahedron Lett., 1988, 29, 5309; Eaton, P.E. and Chakraborthy U.R., J. Am. Chem. Soc., 1978, 100, 3634
   Google Scholar
• Mehta , G. , Srikrishna , A. , Reddy , A. V. and Nair , M. S. 1981 . Tetrahedron , 37 : 4543 (b) Mehta, G., Reddy, A.V. and Srikrishna, A., J. Chem. Soc., Perkin Trans. 1, 1986, 291; Mehta, G., Reddy, A.V. and Srikrishna, A., Indian J. Chem, 1981, 208, 698; Mehta, G., Reddy, A.V. and Srikrishna, A., Tetrahedron Lett., 1979, 4863
   Web of Science ®Google Scholar
• Yoshihira , K. , Fukuoka , M. , Kuroyanagi , M. and Natori , S. 1971 . Chem. Pharm. Bull. , 19 : 1491 Yoshihira, K., Fukuoka, M., Kuroyanagi, M. and Natori, S., Chem. Pharm. Bull., 1972, 20, 426; Nambudiry, M.E.N. and Krishna Rao, G.S., J. Chem. Soc., Perkin Trans. 1, 1974, 317
   Web of Science ®Google Scholar
• Uyehara , T. , Ogata , K. , Yamada , J-I. and Kato , T. 1983 . J. Chem. Soc., Chem. Commun. , For a similar rearrangement with an overall 3,3-shift, see:
   Google Scholar
• Uyehara , T. , Ogata , K. , Yamada , J-I. and Kato , T. 1985 . Bull. Chem. Soc., Jpn. , 58 : 211
   Google Scholar
• In the absence of methanol in the medium, the corresponding ethyl ester was isolated, probably from transesterification with ethyl acetate
   Google Scholar
• Pouchert , C. J. 1983 . The Aldrich Library of NMR spectra , 2nd Ed. , Vol 2 , 13 Milwaukee, WI : Aldrich Chemical Co. inc. .
   Google Scholar