Synthesis of 2,2′-Biindolyls; Potential Intermediates for Indolocarbazole Alkaloids
摘要:
The synthesis of 2,2'-biindolyls oxygenated in the benzenoid ring is reported. Wittig-Horner reaction of the phosphonate esters of 1-benzenesulfonyl-2-bromomethyl-3-substituted indoles with o-nitrobenzaldehydes followed by deoxygenation with triethyl phosphite gave 2,2'-biindolyls.
作者:B. Mohan、D. Nagarathnam、M. Vedachalam、P. C. Srinivasan
DOI:10.1055/s-1985-31150
日期:——
Synthesis of 2,2′-Biindolyls; Potential Intermediates for Indolocarbazole Alkaloids
作者:K. Jesudoss、P. C. Srinivasan
DOI:10.1080/00397919408010172
日期:1994.6
The synthesis of 2,2'-biindolyls oxygenated in the benzenoid ring is reported. Wittig-Horner reaction of the phosphonate esters of 1-benzenesulfonyl-2-bromomethyl-3-substituted indoles with o-nitrobenzaldehydes followed by deoxygenation with triethyl phosphite gave 2,2'-biindolyls.
MOHAN, B.;NAGARATHNAM, D.;VEDACHALAM, M.;SRINIVASAN, P. C., SYNTHESIS, BRD, 1985, N 2, 188-190
作者:MOHAN, B.、NAGARATHNAM, D.、VEDACHALAM, M.、SRINIVASAN, P. C.