478064-32-3Relevant academic research and scientific papers
Fluorous diastereomeric mixture synthesis (FDMS) of hydantoin-fused hexahydrochromeno[4,3-b]pyrroles
Lu, Yimin,Geib, Steven J.,Damodaran, Krishnan,Sui, Bin,Zhang, Zijuan,Curran, Dennis P.,Zhang, Wei
, p. 7578 - 7580 (2010)
Fluorous diastereomeric mixture synthesis (FDMS) is introduced and demonstrated in the synthesis of six diastereomers of hydantoin-fused hexahydrochromeno[4,3-b]pyrroles.
Novel Synthesis of Hexahydrochromeno[4,3-b]pyrrolo[2,1-a]isoquinolines via C-H Functionalization
Dinesha,Mantelingu
, p. 261 - 267 (2019/01/10)
In present work, an efficient and direct method for the synthesis of hexahydrochromeno[4,3-b]pyrrolo[2,1-a]isoquinolines is reported. This method involves T3P mediated oxidation of alcohols to aldehydes followed by [3+2] cycloaddition to afford hexahydroc
PPh3-mediated intramolecular conjugation of alkyl halides with electron-deficient olefins: Facile synthesis of chromans and relevant analogues
Zhu, Jian-Bo,Wang, Peng,Liao, Saihu,Tang, Yong
supporting information, p. 4570 - 4572 (2013/06/04)
With the mediation of phosphine, the direct intramolecular coupling of two electrophiles-alkyl halides with electron-deficient olefins-has been successfully realized in an intramolecular conjugate addition manner. The reaction provides a new approach for
