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1.
Org Lett ; 22(8): 2925-2930, 2020 04 17.
Article in English | MEDLINE | ID: mdl-32233494

ABSTRACT

An enantioselective cyclization of diazoindolinones with o-hydroxymethyl chalcones has been established by a cooperative dirhodium complex and chiral phosphonic acid catalysis under mild conditions. This reaction is the first example of catalytic asymmetric intramolecular Michael-type trapping of oxonium ylide enabled by phosphoric acid through a dual H-bonding activation model, which provides an efficient access to the chiral spirochroman-3,3-oxindoles, with vicinal quaternary and tertiary stereocenters, in good to excellent yields and enantioselectivities.

2.
ACS Omega ; 3(1): 218-228, 2018 Jan 31.
Article in English | MEDLINE | ID: mdl-31457889

ABSTRACT

A chemoselective synthesis of fused novel tricyclic motifs via a facile domino intramolecular cyclization is presented. The strategy enables the formation of dual C-C bond via intramolecular Friedel-Crafts alkylation followed by acylation to accomplish fused tricyclic ketones. Significantly, these fused tricyclic compounds are ubiquitous and constitute major structural cores of natural products.

3.
Org Biomol Chem ; 12(25): 4347-60, 2014 Jul 07.
Article in English | MEDLINE | ID: mdl-24840306

ABSTRACT

Lewis acid (FeCl3) mediated dual bond (C-C and C-O) formation for synthesis of 3,4-dihydrocoumarins is presented. This method has successfully delivered a number of dihydrocoumarins containing dense functionalities on the aromatic ring. Significantly, the present method enabled achieving dihydrocoumarins with tertiary as well as quaternary carbon atoms at the benzylic position. Gratifyingly, the novel spiro-tetracyclic lactones have also been dextrously prepared using this process.


Subject(s)
Chemistry, Organic/methods , Coumarins/chemical synthesis , Lewis Acids/chemistry , Polycyclic Compounds/chemical synthesis , Cinnamates/chemistry , Coumarins/chemistry , Cyclization , Polycyclic Compounds/chemistry , Stereoisomerism
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