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Book ChapterDOI

Thiopyrans and Their Benzo Derivatives

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The article was published on 2020-01-01. It has received 1 citations till now. The article focuses on the topics: Ring (chemistry) & Section (typography).

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δ-Thiolactones as Prodrugs of Thiol-Based Glutamate Carboxypeptidase II (GCPII) Inhibitors

TL;DR: Thiolactones derived from thiol-based glutamate carboxypeptidase II inhibitors exhibited efficacy in a rat model of neuropathic pain following oral administration, consistent with the oral plasma pharmacokinetics.
Journal ArticleDOI

Switching the reactivity of dihydrothiopyran-4-one with aldehydes by aqueous organocatalysis: Baylis-Hillman, aldol, or aldol condensation reactions.

TL;DR: An aqueous medium containing catalytic amounts of a tertiary amine was employed to direct the chemoselectivity of the reaction of aldehydes with 1a to form syn/anti mixtures of 3 with the syn isomers being the major products.
Journal ArticleDOI

Rh-Catalyzed Conjugate Addition of Arylzinc Chlorides to Thiochromones: A Highly Enantioselective Pathway for Accessing Chiral Thioflavanones

TL;DR: This method overcomes catalyst poisoning and substrate inertness and affords a series of chiral thioflavanones (2-arylthiochroman-4-ones) in good yields and with excellent ee values.
Journal ArticleDOI

Highly Enantioselective Conjugate Addition of Ketones to Alkylidene Malonates Catalyzed by a Pyrrolidinyl-Camphor-Derived Organocatalyst

TL;DR: Pyrrolidinyl-camphor derivatives have been proven to be efficient organocatalysts for enantioselective conjugate addition of ketones to alkylidene malonates, affording high chemical yields and high to excellent levels of diastereoselectivity.
Journal ArticleDOI

Recent developments in utility of green multi-component reactions for the efficient synthesis of polysubstituted pyrans, thiopyrans, pyridines, and pyrazoles

TL;DR: Developments made since 2010 in the utilization of multi-component reactions as green efficient methodologies for the synthesis of polysubstituted pyran, thiopyrans, pyridines, and pyrazoles are reviewed and the mechanisms of these processes are discussed.