927210-83-1Relevant academic research and scientific papers
A general synthetic entry to the pentacyclic Strychnos alkaloid family, using a [4 + 2]-cycloaddition/rearrangement cascade sequence
Boonsombat, Jutatip,Zhang, Hongjun,Chughtai, Majid J.,Hartung, John,Padwa, Albert
, p. 3539 - 3550 (2008)
(Chemical Equation Presented) The total synthesis of (±)- strychnopivotine, (±)-tubifolidine, (±)-strychnine, and (±)-valparicine is reported. The central step in the synthesis consists of an intramolecular [4 + 2]-cycloaddition/rearrangement cascade of a
Total synthesis of (±)-strychnine via a [4 + 2]-cycloaddition/ rearrangement cascade
Zhang, Hongjun,Boonsombat, Jutatip,Padwa, Albert
, p. 279 - 282 (2007)
(Chemical Equation Presented) A new strategy for the synthesis of the Strychnos alkaloid (±)-strychnine has been developed and is based on an intramolecular [4 + 2]-cycloaddition/rearrangement cascade of an indolyl-substituted amidofuran. The critical D-r
