Intramolecular Diels-Alder reaction as a key step in tandem or sequential processes: a versatile tool for the synthesis of fused and bridged bicyclic or polycyclic compounds

Article ID	Journal	Published Year	Pages	File Type
5216711	Tetrahedron	2014	32 Pages	PDF

Keywords

PIFA TFA MOB MSA DMP DCC DCB NOE PMB DMAP PDC DDQ IMDA benzyloxymethyl THF PIDA BHT p-TsOH TBDPS DCE EDDA 1,3,5-Triisopropylbenzene IBX para-methoxybenzyl DIBA nuclear magnetic resonance 1,2-dichloroethane 1,2-Dichlorobenzene 1,3-dicyclohexylcarbodiimide 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone 4-(N,N-dimethylamino)pyridine Dess–Martin periodinane DFT Intramolecular Diels–Alder DMSO N,N-diisopropylethylamine Trifluoroacetic acid Methanesulfonic acid camphorsulfonic acid CSA Sequential butylated hydroxy toluene Tetrahydrofuran tert-butyldiphenylsilyl tert-butyldimethylsilyl triethylamine NMR nuclear Overhauser enhancement Bom Diels–Alder Tandem pyridinium dichromate Diacetoxyiodobenzene Dimethyl sulfoxide Natural product microwave DIPEA Density functional theory TEA One-pot

Related Topics

Physical Sciences and Engineering Chemistry Organic Chemistry

Intramolecular Diels-Alder reaction as a key step in tandem or sequential processes: a versatile tool for the synthesis of fused and bridged bicyclic or polycyclic compounds

Authors

Prakash T. Parvatkar, Hari K. Kadam, Santosh G. Tilve,