A revised modular approach to various synthetic (–)-trans-Δ 8 -THC derivatives through late-stage Suzuki–Miyaura cross-coupling reactions is disclosed. Ten derivatives were synthesized allowing both sp 2 - and sp 3 -hybridized cross-coupling partners with minimal β-hydride elimination. Importantly, we demonstrate that a para-bromo-substituted THC scaffold for Suzuki–Miyaura cross-coupling reactions has been initially reported incorrectly in recent literature. </p
We describe the synthesis of 8-heteroaromatic-2'-deoxyguanosine analogues using Suzuki-Miyaura or St...
Novel rigid 8-biaryl-2'-deoxyadenosines with tuneable fluorescent properties can be accessed by an e...
New methodology is described to construct the olefinic bond in overcrowded alkenes using a hypervale...
A revised modular approach to various synthetic (–)-trans-Δ 8 -THC derivatives through late-stage S...
A revised modular approach to various synthetic (–)-trans-Δ 8 -THC derivatives through late-stage Su...
A revised modular approach to various synthetic (–)-trans-Δ8-THC derivatives through late-stage Suzu...
A revised modular approach to various synthetic (–)-trans-Δ8-THC derivatives through late-stage Suzu...
In this manuscript we describe a modular pathway to synthesize biologically relevant (–)-trans-Δ8-TH...
Vinyliodide reacts chemoselectively under Heck–Mizoroki conditions with terminal alkenes, including ...
Vinyliodide reacts chemoselectively under Heck–Mizoroki conditions with terminal alkenes, including ...
A number of aryl building blocks for the synthesis of two xanthomonadin natural product pigments, as...
Approaches to the polyene natural product xanthomonadin, an octaenyl electron-deficient bacterial ph...
The development and study of new solvents has become important due to a proliferation of regulations...
A number of aryl building blocks for the synthesis of two xanthomonadin natural product pigments, as...
Synthetic routes to two molecular motors are reported. The sterically hindered central olefinic bond...
We describe the synthesis of 8-heteroaromatic-2'-deoxyguanosine analogues using Suzuki-Miyaura or St...
Novel rigid 8-biaryl-2'-deoxyadenosines with tuneable fluorescent properties can be accessed by an e...
New methodology is described to construct the olefinic bond in overcrowded alkenes using a hypervale...
A revised modular approach to various synthetic (–)-trans-Δ 8 -THC derivatives through late-stage S...
A revised modular approach to various synthetic (–)-trans-Δ 8 -THC derivatives through late-stage Su...
A revised modular approach to various synthetic (–)-trans-Δ8-THC derivatives through late-stage Suzu...
A revised modular approach to various synthetic (–)-trans-Δ8-THC derivatives through late-stage Suzu...
In this manuscript we describe a modular pathway to synthesize biologically relevant (–)-trans-Δ8-TH...
Vinyliodide reacts chemoselectively under Heck–Mizoroki conditions with terminal alkenes, including ...
Vinyliodide reacts chemoselectively under Heck–Mizoroki conditions with terminal alkenes, including ...
A number of aryl building blocks for the synthesis of two xanthomonadin natural product pigments, as...
Approaches to the polyene natural product xanthomonadin, an octaenyl electron-deficient bacterial ph...
The development and study of new solvents has become important due to a proliferation of regulations...
A number of aryl building blocks for the synthesis of two xanthomonadin natural product pigments, as...
Synthetic routes to two molecular motors are reported. The sterically hindered central olefinic bond...
We describe the synthesis of 8-heteroaromatic-2'-deoxyguanosine analogues using Suzuki-Miyaura or St...
Novel rigid 8-biaryl-2'-deoxyadenosines with tuneable fluorescent properties can be accessed by an e...
New methodology is described to construct the olefinic bond in overcrowded alkenes using a hypervale...