M. Yasuda

Streptonigrin and lavendamycin partial structures. Probes for the minimum, potent pharmacophore of streptonigrin, lavendamycin, and synthetic quinoline-5,8-diones.

Inverse electron demand Diels-Alder reactions of heterocyclic azadienes. Studies on the total synthesis of lavendamycin: investigative studies on the preparation of the CDE .beta.-carboline ring system and AB quinoline-5,8-quinone ring system

Total synthesis of lavendamycin methyl ester

Substituent effects in [2.sigma. + 2.sigma. + 2.sigma.] thermal decarbonylation of cage ketones. Remarkably effective elongation of strained carbon-carbon bond by through-bond coupling

Streptonigrin and lavendamycin partial structures. Preparation of 7-amino-2-(2′-pyridyl)quinoline-5,8-quinone-6′-carboxylic acid: A probe for the minimum, potent pharmacophore of the naturally occurring antitumor-antibiotics

An improved and divergent introduction of the streptonigrin and lavendamycin quinoline 5 8 quinone ab ring systems

Additions and Corrections - Frontier-Controlled Cycloaddition Reactions of Phencyclone with Electron-Rich Dienophiles via Charge-Transfer Complexes: Kinetic Study and Its Mechanistic Aspects.

Frontier-controlled pericyclic reaction of phencyclone with 1H-azepine. Remarkably accelerated aromatic Cope reaarangement of an endo-[4 + 2]-.pi. cycloadduct

Preparation and Inverse‐Electron‐Demand Diels–Alder Reaction of an Electron‐Deficient Heterocyclic Azadiene: Triethyl 1,2,4‐Triazine‐3,5,6‐Tricarboxylate and 2,3,6‐Tricarboethoxypyridine

Inverse Electron Demand Diels-Alder Reactions of Heterocyclic Aza Dienes.