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1.
Chemistry ; 28(71): e202202383, 2022 Dec 20.
Article in English | MEDLINE | ID: mdl-36081382

ABSTRACT

Garsubellin A is a thirty-carbon meroterpenoid capable of enhancing the enzyme choline acetyltransferase whose decreased level is associated with the symptoms of Alzheimer's disease. Due to the potentially useful biological activity along with the novel molecular architecture, this plant metabolite has remained a popular synthetic target. Herein we report a full account of our synthetic investigations that have led to the enantioselective total synthesis of garsubellin A, establishing its absolute stereostructure. The protecting group-free, twelve-step synthetic route has enabled the syntheses of the natural (-)-garsubellin A and its unnatural (+)-antipode.


Subject(s)
Alzheimer Disease , Biological Products , Humans , Stereoisomerism , Terpenes/chemistry , Choline O-Acetyltransferase/metabolism
2.
Angew Chem Int Ed Engl ; 60(42): 22735-22739, 2021 10 11.
Article in English | MEDLINE | ID: mdl-34398517

ABSTRACT

Garsubellin A is a meroterpene capable of enhancing the enzyme choline acetyltransferase whose decreased level is believed to play a central role in the symptoms of Alzheimer's disease. Due to the potentially useful biological activity together with the novel bridged and fused cyclic molecular architecture, garsubellin A has garnered substantial synthetic interest, but its absolute stereostructure has been undetermined. We report here the first enantioselective total synthesis of (+)-garsubellin A. Our synthesis relies on stereoselective fashioning of a cyclohexanone framework and double conjugate addition of 1,2-ethanedithiol that promotes aldol cyclization to build the bicyclic [3.3.1] skeleton. The twelve-step, protecting group-free synthetic route has enabled the syntheses of both the natural (-)-garsubellin A and its unnatural (+)-antipode for biological evaluations.


Subject(s)
Terpenes/chemical synthesis , Biological Products/chemical synthesis , Biological Products/chemistry , Bridged Bicyclo Compounds/chemistry , Crystallography, X-Ray , Cyclization , Molecular Conformation , Stereoisomerism , Terpenes/chemistry
3.
Nanotechnology ; 24(31): 315502, 2013 Aug 09.
Article in English | MEDLINE | ID: mdl-23851670

ABSTRACT

A high performance, stretchable UV sensor array was fabricated based on an active matrix (AM) device that combined field effect transistors of SWCNTs and SnO2 nanowires. The AM devices provided spatial UV sensing via the individual sensors in the array. SnO2 NW UV sensors showed an average photosensitivity of ∼10(5) and a photoconductive gain of ∼10(6) under very low UV (λ = 254 nm) power intensities of 0.02-0.04 mW cm(-2). The UV sensing performance was not deteriorated by a prestrain of up to 23% induced by radial deformation, consistent with the mechanical analysis.

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