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Sasaki, M., Hamzik, P.J., Ikemoto, H., Bartko, S.G. and Danheiser, R.L. (2018) Formal Bimolecular [2 + 2 + 2] Cycloaddition Strategy for the .Synthesis of Pyridines: Intramolecular Propargylic Ene Reaction/Aza Diels-Alder Reaction Cascades. Organic Letters, 20, 6244-6249.
https://doi.org/10.1021/acs.orglett.8b02728

has been cited by the following article:

• TITLE: Rhodium Catalyzed [2π + 2π + 2π]-Cycloaddition of Alkynyl-Ynamides and Carbon Disulfide to Indolo-Thiopyrane Thiones

  AUTHORS: Benjamin Dassonneville, Felix Hinkel, Heiner Detert

  KEYWORDS: Cycloaddition, Heterocycles, Rhodium, Sulfur, Alkyne

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.13 No.1, March 14, 2023

  ABSTRACT: The synthesis of new indoloannulated thiopyranethiones is reported. The key-step is a rhodium-catalyzed [2 + 2 + 2]-cycloaddition of alkynyl-ynamides with carbon disulfide to close the pyrrole and the thiopyranethione rings simultaneously. A violet idolothiopyrane thione or a mixture of the violet and a red isomer result from [RhCl(C8H14)2]2/3BINAP catalyzed cycloadditions, the regiochemistry is controlled by the substitution pattern on the alkynyl-ynamide.