A PPh<sub>3</sub> mediated reductive annulation reaction between isatins and 4,4-dicyano-2-methylenebut-3-enoates was developed. The reaction provided an alternative method for constructing five- and three-membered all-carbon spirooxindole compounds. Lithium chloride as a Lewis acid played a key role in the synthesis of spirocyclopentenyl oxindole compounds
Spirocyclopentene Oxindoles through LiHMDS Based Allylation and Ring Closing Metathesi
A two-step one-pot efficient synthesis of pyrido[2,3-b]indoles via reaction between isatin, α-amin...
Spirocyclopentene Oxindoles through LiHMDS Based Allylation and Ring Closing Metathesi
<p>An efficient molecular hybridization strategy has been utilized for the synthesis of pirooxindole...
Under the cooperative catalysis of NHC/Lewis acid, the mild, straightforward [4 + 2] annulation of α...
A variety of spirolactones are prepared from cyclic anhydrides via indium-mediated allylation and ri...
Lewis acid catalyzed highly efficient [3+2] annulation of spirocyclic Donor-Acceptor cyclopropanes (...
Lewis acid catalyzed highly efficient [3+2] annulation of spirocyclic Donor-Acceptor cyclopropanes (...
A mild and practical synthesis of spirooxindole [1,3]oxazino derivatives from N-substituted isatins ...
A simple and one-pot protocol for the synthesis of indene-spiro-oxindole derivatives via TiCl<SUB>4<...
International audienceAn efficient, simple, and convenient synthetic procedure for the synthesis of ...
International audienceAn efficient, simple, and convenient synthetic procedure for the synthesis of ...
International audienceAn efficient, simple, and convenient synthetic procedure for the synthesis of ...
International audienceAn efficient, simple, and convenient synthetic procedure for the synthesis of ...
International audienceAn efficient, simple, and convenient synthetic procedure for the synthesis of ...
Spirocyclopentene Oxindoles through LiHMDS Based Allylation and Ring Closing Metathesi
A two-step one-pot efficient synthesis of pyrido[2,3-b]indoles via reaction between isatin, α-amin...
Spirocyclopentene Oxindoles through LiHMDS Based Allylation and Ring Closing Metathesi
<p>An efficient molecular hybridization strategy has been utilized for the synthesis of pirooxindole...
Under the cooperative catalysis of NHC/Lewis acid, the mild, straightforward [4 + 2] annulation of α...
A variety of spirolactones are prepared from cyclic anhydrides via indium-mediated allylation and ri...
Lewis acid catalyzed highly efficient [3+2] annulation of spirocyclic Donor-Acceptor cyclopropanes (...
Lewis acid catalyzed highly efficient [3+2] annulation of spirocyclic Donor-Acceptor cyclopropanes (...
A mild and practical synthesis of spirooxindole [1,3]oxazino derivatives from N-substituted isatins ...
A simple and one-pot protocol for the synthesis of indene-spiro-oxindole derivatives via TiCl<SUB>4<...
International audienceAn efficient, simple, and convenient synthetic procedure for the synthesis of ...
International audienceAn efficient, simple, and convenient synthetic procedure for the synthesis of ...
International audienceAn efficient, simple, and convenient synthetic procedure for the synthesis of ...
International audienceAn efficient, simple, and convenient synthetic procedure for the synthesis of ...
International audienceAn efficient, simple, and convenient synthetic procedure for the synthesis of ...
Spirocyclopentene Oxindoles through LiHMDS Based Allylation and Ring Closing Metathesi
A two-step one-pot efficient synthesis of pyrido[2,3-b]indoles via reaction between isatin, α-amin...
Spirocyclopentene Oxindoles through LiHMDS Based Allylation and Ring Closing Metathesi