@article {48703, title = {Radical cascade cyclization of unactivated alkene-tethered indoles with aryldiazonium salt and sodium metabisulfite to access Azo- and Sulfonylated-2,3-Dihyro-1H-pyrrolo[1,2-a]indoles}, journal = {Journal of Organic Chemistry}, volume = {88}, year = {2023}, month = {JUN}, pages = {9123-9129}, type = {Article}, abstract = {

A method for the construction ofheterocyclic scaffold2,3-dihyro-1H-pyrrolo[1,2-a]indolesvia arylsulfonylradical-triggered cascade cyclization of unactivated alkene-tetheredindoles in the absence of any external photocatalyst has been developed.This protocol features easily accessible starting materials such assodium metabisulfite and aryldiazonium tetrafluoroborates at roomtemperature and offers good functional group compatibility, enablingthe introduction of various functionalized sulfonyl and azo groupsinto pyrrolo[1,2-a]indoles.

}, issn = {0022-3263}, doi = {10.1021/acs.joc.3c00759}, author = {Kumar, Pawan and Rai, Archana and Kumar, Manish and Krishna, Gamidi Rama and Das, Utpal} } @article {49650, title = {Reaction of 4 (Alkynyloxy)cyclohexa-2,5-dienones with Dimethyl Sulfoxide: a catalyst-free formation of 6/5/3-fused tricyclic enones}, journal = {Journal of Organic Chemistry}, volume = {90}, year = {2024}, month = {DEC}, pages = {653-657}, type = {article}, abstract = {

6/5/3-Fused tricyclic enones were obtained when 4-(alkynyloxy)cyclohexa-2,5-dienones were treated with DMSO at 150 {\textdegree}C. The reaction proceeded via a four-membered oxathietene intermediate. The protocol developed is atom economical, has a broad substrate scope, and is amenable to gram-scale synthesis. The products obtained are susceptible to further synthetic transformations.

}, doi = {https://doi.org/10.1021/acs.joc.4c02553}, author = {Rai, Archana and Das, Utpal} }