Herein, we report a transition-metal-free annulation reaction of benzynes and 1,3-oxopentanedioate for the synthesis of highly functionalized naphthalene derivatives for the first time. Additionally, the representative naphthalene derivatives have been successfully transformed into the new series of rhodamine dye analogues
An unexpected rearrangement aromatization of benzo[<i>c</i>]oxepine has been revealed to synthesize ...
We report a visible-light-promoted synthesis of substituted naphthalenes via [4 + 2] annulation of a...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
Herein, we report a transition-metal-free annulation reaction of benzynes and 1,3-oxopentanedioate f...
A transition-metal-free coupling annulation reaction of arynes, ketones, and alkynoates has been dem...
A series of functionalized 1-amino-2-naphthalenecarboxylic acid derivatives were synthesized from en...
An interesting σ-bond insertion/benzannulation reaction for the synthesis of polysubstituted naphtha...
A mild and transition-metal-free one-pot strategy is established to prepare polysubstituted naphthal...
Arynes are known as useful synthons in organic synthesis. In particular, reactions accompanying mult...
The highly monoselective N-arylation of aromatic tertiary amines using a transition-metal-free appro...
A new one-pot synthetic route to achieve the preparation of hydroxy and amine binaphthyl and biphena...
An efficient and redox-neutral naphthol synthesis has been realized via rhodium(III) catalyzed C-H a...
A rhodium(III)-catalyzed direct dehydrogenative annulation of benzamides with alkynes through chelat...
A facile formal synthesis to aphanorphine and its analogue is described, featuring Rh-catalyzed cycl...
Arynes are known as useful synthons in organic synthesis. In particular, reactions accompanying mult...
An unexpected rearrangement aromatization of benzo[<i>c</i>]oxepine has been revealed to synthesize ...
We report a visible-light-promoted synthesis of substituted naphthalenes via [4 + 2] annulation of a...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
Herein, we report a transition-metal-free annulation reaction of benzynes and 1,3-oxopentanedioate f...
A transition-metal-free coupling annulation reaction of arynes, ketones, and alkynoates has been dem...
A series of functionalized 1-amino-2-naphthalenecarboxylic acid derivatives were synthesized from en...
An interesting σ-bond insertion/benzannulation reaction for the synthesis of polysubstituted naphtha...
A mild and transition-metal-free one-pot strategy is established to prepare polysubstituted naphthal...
Arynes are known as useful synthons in organic synthesis. In particular, reactions accompanying mult...
The highly monoselective N-arylation of aromatic tertiary amines using a transition-metal-free appro...
A new one-pot synthetic route to achieve the preparation of hydroxy and amine binaphthyl and biphena...
An efficient and redox-neutral naphthol synthesis has been realized via rhodium(III) catalyzed C-H a...
A rhodium(III)-catalyzed direct dehydrogenative annulation of benzamides with alkynes through chelat...
A facile formal synthesis to aphanorphine and its analogue is described, featuring Rh-catalyzed cycl...
Arynes are known as useful synthons in organic synthesis. In particular, reactions accompanying mult...
An unexpected rearrangement aromatization of benzo[<i>c</i>]oxepine has been revealed to synthesize ...
We report a visible-light-promoted synthesis of substituted naphthalenes via [4 + 2] annulation of a...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...