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Conjugated Thiophene-Fused Isatin Dyes through Intramolecular Direct Arylation
We report on the design, synthesis, and properties of innovative, planar, π-conjugated compounds in which a thiophene ring is fused with the skeleton of the naturally occurring... -
Ortho-Substituted Catechol Derivatives: The Effect of Intramolecular Hydroge...
This paper reports a series of chloride anion receptors containing two catechol head groups connected through their ortho-positions via a spacer chain. The linking group chosen... -
Total Synthesis of Phomactin A
A total synthesis of (±)-phomactin A is described to highlight the final completion of a complex natural product target that had commenced with an intramolecular oxa-[3 + 3]... -
Enantioselective Intramolecular Aromatic [4 + 4] Photocycloaddition in Crysta...
Photoreactivity of seven 9-anthryl-N-(naphthylcarbonyl)carboxamide derivatives, 1a−g, in their intramolecular [4 + 4] photocycloadditions in solid state is discussed on the... -
r37980778c78--d76f00a1e2f52739f928d39a4f530b57
One-pot coupling of an intramolecular thermal [5C + 2C] pyrone−alkene cycloaddition to a [4C + 2C] Diels−Alder reaction provides immediate access to 6,7,5-tricarbocyclic systems... -
r37980778c78--80e78074aeeddb0d3ba0918fd3411e55
A total synthesis of (±)-phomactin A is described to highlight the final completion of a complex natural product target that had commenced with an intramolecular oxa-[3 + 3]... -
r37980778c78--e7976c4138e67fee2a4573aae0e36321
A series of bis-iminonitroxide diradical derivatives of different lengths and geometry have been prepared that incorporate a conjugated phenylene-ethynylene bridge as a rigid... -
Ortho-Substituted Catechol Derivatives: The Effect of Intramolecular Hydroge...
This paper reports a series of chloride anion receptors containing two catechol head groups connected through their ortho-positions via a spacer chain. The linking group chosen... -
Revisiting the Ullmann−Ether Reaction: A Concise and Amenable Synthesis of N...
A concise synthesis of a series of novel dibenzoxepino[4,5-d]pyrazoles was accomplished by implementation of an intramolecular Ullmann-ether reaction on... -
r37980778c78--5ff34496ad0852736827049274b83b40
The total synthesis of VM55599, a natural metabolite of Penicillium sp. IMI332995, has been achieved via an intramolecular Diels−Alder cycloaddition of a reverse isoprene moiety... -
Synthesis of the Putative Structure of Eupomatilone-6
The synthesis of eupomatilone-6 (1) has been achieved by using Suzuki coupling, Sharpless asymmetric dihydroxylation, and intramolecular Horner−Wadsworth−Emmons reactions. The...
