We report a general visible-light-mediated strategy that enables the construction of complex C(sp3)-rich N-heterospirocycles from feedstock aliphatic ketones and aldehydes with a broad selection of alkene-containing secondary amines. Key to the success of this approach was the utilization of a highly reducing Ir-photocatalyst and orchestration of the intrinsic reactivities of 1,4-cyclohexadiene and Hantzsch ester. This methodology provides streamlined access to complex C(sp3)-rich N-heterospirocycles displaying structural and functional features relevant to fragment-based lead identification programs.We are grateful to the Gates Cambridge Trust (N.J.F.) and Herchel Smith Scholarship Scheme (A.T.) for studentships, the EPSRC (EP/S020292/1 an...
Alkylations of simple electron‐rich heterocompounds deliver valuable target structures in bioorganic...
International audienceA new strategy from simple cyclic β-ketoesters or amides involving a selective...
International audienceA new strategy from simple cyclic β-ketoesters or amides involving a selective...
We report a general visible-light-mediated strategy that enables the construction of complex C(sp3)-...
We report a general visible-light-mediated strategy that enables the construction of complex C(sp3)...
We report a general visible-light-mediated strategy that enables the construction of complex C(sp3)...
We report a general visible-light-mediated strategy that enables the construction of complex C(sp3)...
Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tri...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
© 2021 Tyra Hayley HorngrenThe three-dimensional structure of proteins and receptor binding sites re...
Natural products remain the most common source for drug leads, although diversity-oriented synthesis...
Alkylations of simple electron‐rich heterocompounds deliver valuable target structures in bioorganic...
Alkylations of simple electron‐rich heterocompounds deliver valuable target structures in bioorganic...
International audienceA new strategy from simple cyclic β-ketoesters or amides involving a selective...
International audienceA new strategy from simple cyclic β-ketoesters or amides involving a selective...
We report a general visible-light-mediated strategy that enables the construction of complex C(sp3)-...
We report a general visible-light-mediated strategy that enables the construction of complex C(sp3)...
We report a general visible-light-mediated strategy that enables the construction of complex C(sp3)...
We report a general visible-light-mediated strategy that enables the construction of complex C(sp3)...
Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tri...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
© 2021 Tyra Hayley HorngrenThe three-dimensional structure of proteins and receptor binding sites re...
Natural products remain the most common source for drug leads, although diversity-oriented synthesis...
Alkylations of simple electron‐rich heterocompounds deliver valuable target structures in bioorganic...
Alkylations of simple electron‐rich heterocompounds deliver valuable target structures in bioorganic...
International audienceA new strategy from simple cyclic β-ketoesters or amides involving a selective...
International audienceA new strategy from simple cyclic β-ketoesters or amides involving a selective...