Efficient access to enantiopure 1,3-disubstituted isoindolines from selective catalytic fragmentation of an original desymmetrized rigid overbred template

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Aza-Quaternary Scaffolds from Selective Bond Cleavage of Bridgehead-Substituted 7-Azabicyclo[2.2.1]heptane: Total Synthesis of (+)-Cylindricines C-E and (-)-Lepadiformine A.Crystal Structure, Spectroscopy, SEM Analysis, and Computational Studies of N-(1,3-Dioxoisoindolin-2yl)benzamide

P2860

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P2860

Efficient access to enantiopure 1,3-disubstituted isoindolines from selective catalytic fragmentation of an original desymmetrized rigid overbred template

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http://www.wikidata.org/entity/Q29031161

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Efficient access to enantiopur ...... trized rigid overbred template

@ast

Efficient access to enantiopur ...... trized rigid overbred template

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Efficient access to enantiopur ...... trized rigid overbred template

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Efficient access to enantiopur ...... trized rigid overbred template

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Efficient access to enantiopur ...... trized rigid overbred template

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Efficient access to enantiopur ...... trized rigid overbred template

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P1476

Efficient access to enantiopur ...... trized rigid overbred template

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P2093

Divya Tiwari

http://www.w3.org/2001/XMLSchema#string

Ganesh Pandey

http://www.w3.org/2001/XMLSchema#string

Rajesh Varkhedkar

http://www.w3.org/2001/XMLSchema#string

P2860

Dihydroxyphenylisoindoline amides as orally bioavailable inhibitors of the heat shock protein 90 (hsp90) molecular chaperone

Discovery of isoindoline and tetrahydroisoquinoline derivatives as potent, selective PPARδ agonists

Synthesis of novel angiotensin converting enzyme inhibitor quinapril and related compounds. A divergence of structure-activity relationships for non-sulfhydryl and sulfhydryl types.

RETRACTED: A novel class of specific Hsp90 small molecule inhibitors demonstrate in vitro and in vivo anti-tumor activity in human melanoma cells.

Structure-activity relationship studies on isoindoline inhibitors of dipeptidyl peptidases 8 and 9 (DPP8, DPP9): is DPP8-selectivity an attainable goal?

Synthesis of ent-kaurane and beyerane diterpenoids by controlled fragmentations of overbred intermediates.

Selective non-nucleoside HIV-1 reverse transcriptase inhibitors. New 2,3-dihydrothiazolo[2,3-a]isoindol-5(9bH)-ones and related compounds with anti-HIV-1 activity.

Tandem nucleophilic addition-intramolecular aza-Michael reaction: facile synthesis of chiral fluorinated isoindolines.

1,3-Diaryl-4,5,6,7-tetrahydro-2H-isoindole derivatives: a new series of potent and selective COX-2 inhibitors in which a sulfonyl group is not a structural requisite.

Structural features of aliphatic N-nitrosamines of 7-azabicyclo[2.2.1]heptanes that facilitate N-NO bond cleavage.

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4438-4448

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scholarly article

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10.1039/C5OB00229J

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P478

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2015-01-01T00:00:00Z

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25764985

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Efficient access to enantiopure 1,3-disubstituted isoindolines from selective catalytic fragmentation of an original desymmetrized rigid overbred template

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P2860

P2860

Efficient access to enantiopure 1,3-disubstituted isoindolines from selective catalytic fragmentation of an original desymmetrized rigid overbred template

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type

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P1433

P1476

P2093

P2860

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P698

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P1433

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P2860

P304

P31

P356

P433

P478

P577

P698