36 research outputs found
Heavier alkaline earth catalyzed ene-yne cyclizations:Atom-efficient access to tetrahydroisoquinoline frameworks
Short and Efficient Syntheses of Protoberberine Alkaloids using Palladium-Catalyzed Enolate Arylation
A concise synthesis of the biologically active alkaloid berberine is reported, and a versatile palladiumācatalyzed enolate arylation is used to form the isoquinoline core. The overall yield of 50ā% is a large improvement over the single, previous synthesis. By design, this modular route allows the rapid synthesis of other members of the protoberberine family (e.g., pseudocoptisine and palmatine) by substitution of the readily available aryl bromide and ketone coupling partners. Moreover, by combining enolate arylation with inā
situ functionalization, substituents can be rapidly and regioselectively introduced at the alkaloid C13 position, as demonstrated by the total synthesis of dehydrocorydaline. The avoidance of electrophilic aromatic substitution reactions to make the isoquinoline allows direct access to analogues possessing more varied electronic properties, such as the fluorineācontaining derivative synthesized here
Synthesis of Functionalized Pyridines via a Regioselective Oxazoline Promoted CH Amidation Reaction
An Extremely Powerful Acylation Reaction of Alcohols with Acid Anhydrides Catalyzed by Trimethylsilyl Trifluoromethanesulfonate ā
Lead identification of benzimidazolone and azabenzimidazolone arylsulfonamides as CC-chemokine receptor 4 (CCR4) antagonists
A knowledge-based library of 2,3-dichlorophenylsulfonyl derivatives of commercially available aryl amines was synthesised and screened as human CCR4 antagonists, in order to identify a suitable hit for the start of a lead-optimisation programme. Hits were required to be more potent than an existing indazole series, have better physicochemical properties (c log P 116 Ī¼g/mL), and be stable to acid and light. The benzimidazol-2-one core was identified as a hit suitable for further investigation. Substitution at N1 with small alkyl groups was tolerated; however, these analogues were inactive in the whole blood assay (pA2 <5). Azabenzimidazolone analogues were all found to be active, with compound 38 exhibiting whole blood activity of 6.1, low molecular weight (389) and chrom log D7.4 (2.4), high LE (0.43), and solubility (152 Ī¼g/mL). In addition, 38 had human serum albumin binding of around 93% and met all the criteria for progression to lead optimisation
Rearrangement of a 16Ī±,17Ī±-Epoxy-16Ī²-methylandrostane-17Ī²-carbothioic Acid to a 17Ī²-Mercapto-16Ī²-methylandrostane-17Ī±,16Ī±-carbolactone
Heavier Alkaline Earth Catalyzed Ene-yne Cyclizations: Atom-Efficient Access to Tetrahydroisoquinoline Frameworks
Tetrahydroisoquinoline
frameworks may be accessed with 100% atom
efficiency through the alkaline earth catalyzed addition of primary
amines to ene-yne substrates through a sequence of intermolecular
alkene and intramolecular alkyne hydroamination steps
Heavier Alkaline Earth Catalysts for the Intermolecular Hydroamination of Vinylarenes, Dienes, and Alkynes
The heavier group 2 complexes [MĀ{NĀ(SiMe<sub>3</sub>)<sub>2</sub>}<sub>2</sub>]<sub>2</sub> (<b>1</b>, M = Ca; <b>2</b>, M = Sr) and [MĀ{CHĀ(SiMe<sub>3</sub>)<sub>2</sub>}<sub>2</sub>(THF)<sub>2</sub>] (<b>3</b>, M = Ca; <b>4</b>, M = Sr)
are shown
to be effective precatalysts for the intermolecular hydroamination
of vinyl arenes and dienes under mild conditions. Initial studies
revealed that the amide precatalysts, <b>1</b> and <b>2</b>, while compromised in terms of absolute activity by a tendency toward
transaminative behavior, offer greater stability toward polymerization/oligomerization
side reactions. In every case the strontium species, <b>2</b> and <b>4</b>, were found to outperform their calcium congeners.
Reactions of piperidine with <i>para</i>-substituted styrenes
are indicative of rate-determining alkene insertion in the catalytic
cycle while the ease of addition of secondary cyclic amines was found
to be dependent on ring size and reasoned to be a consequence of varying
amine nucleophilicity. Hydroamination of conjugated dienes yielded
isomeric products via Ī·<sup>3</sup>-allyl intermediates and
their relative distributions were explained through stereoelectronic
considerations. The ability to carry out the hydroamination of internal
alkynes was found to be dramatically dependent upon the identity of
the alkyne substituents while reactions employing terminal alkynes
resulted in the precipitation of insoluble and unreactive group 2
acetylides. The rate law for styrene hydroamination with piperidine
catalyzed by [SrĀ{NĀ(SiMe<sub>3</sub>)<sub>2</sub>}<sub>2</sub>]<sub>2</sub> was deduced to be first order in [amine] and [alkene] and
second order in [catalyst], while large kinetic isotope effects and
group 2 element-dependent Ī<i>S</i><sup>ā§§</sup> values implicated the formation of an amine-assisted rate-determining
alkene insertion transition state in which there is a considerable
entropic advantage associated with use of the larger strontium center