https://pubs.rsc.org/en/content/articlepdf/2019/NP/C8NP00092A

Marine natural products.

Bile salt biotransformations by human intestinal bacteria.

Electrochemistry represents one of the most intimate ways of interacting with molecules. This review discusses advances in synthetic organic electrochemistry since 2000. Enabling methods and synthetic applications are analyzed alongside innate advantages as well as future challenges of electroorganic chemistry.

Synthetic Organic Electrochemical Methods Since 2000: On the Verge of a Renaissance

Recent developments in the chemistry of halogen-free flame retardant polymers

1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis

The stereochemistry and synthetic utility of the addition of 2-(trimethylsilyl)thiazole (2-TST, 1) to various N-protected α-amino aldehydes is described. The reactions of 1 with n-Boc-L-serinal acetonide (2) and N-Boc-L-threoninal acetonide (3) are essentially anti diastereoselective (ds=85-90%) in agreement with the Felkin-Anh model for asymmetric induction, whereas the reactions with O-benzyl-NH-Boc-L-serinal (4) and NH-Boc-L-phenylalaninal (5) are syn diastereoselective (ds=80%). The reversal of diastereoselectivity is interpreted on the basis of a proton-bridged cyclic Cram model for asymmetric induction

Stereochemistry associated with the addition of 2-(trimethylsilyl)thiazole to differentially protected .alpha.-amino aldehydes. Applications toward the synthesis of amino sugars and sphingosines

Use of moss (Tortula muralis Hedw.) for monitoring organic and inorganic air pollution in urban and rural sites in Northern Italy

Synthese par lithiation/silylation du thiazole; reactions avec des cetenes, chlorures d'acyle et aldehydes

Synthesis of (trimethylsilyl)thiazoles and reactions with carbonyl compounds. Selectivity aspects and synthetic utility

Iterative, stereoselective homologation of chiral polyalkoxy aldehydes employing 2-(trimethylsilyl)thiazole as a formyl anion equivalent. The thiazole route to higher carbohydrates

Hexakis(4-hydroxyphenoxy)cyclophosphazene and poly[bis(4-hydroxyphenoxy)phosphazene] are synthesized by reaction of 4-methoxyphenoxy-substituted cyclo- and polyphosphazenes with an excess of BBr 3 . An alternative method is based on a Pd-catalyzed hydrogenation under pressure of other phosphazene substrates bearing4-(benzyloxy)phenoxy substituents

Paola Pedrini

Papers

Stereochemistry associated with the addition of 2-(trimethylsilyl)thiazole to differentially protected .alpha.-amino aldehydes. Applications toward the synthesis of amino sugars and sphingosines

Use of moss (Tortula muralis Hedw.) for monitoring organic and inorganic air pollution in urban and rural sites in Northern Italy

Synthesis of (trimethylsilyl)thiazoles and reactions with carbonyl compounds. Selectivity aspects and synthetic utility

Iterative, stereoselective homologation of chiral polyalkoxy aldehydes employing 2-(trimethylsilyl)thiazole as a formyl anion equivalent. The thiazole route to higher carbohydrates

Functionalization of phosphazenes. 1. Synthesis of phosphazene materials containing hydroxyl groups