An Enantio- and Diastereocontrolled Synthesis of (–)-Salinosporamide A

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Pharmacodynamic and efficacy studies of the novel proteasome inhibitor NPI-0052 (marizomib) in a human plasmacytoma xenograft murine model

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A1,3-strain enabled retention of chirality during bis-cyclization of β-ketoamides: total synthesis of (−)-salinosporamide A and (−)-homosalinosporamide A

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Concise Formal Synthesis of (−)-Salinosporamide A (Marizomib) Using a Regio- and Stereoselective Epoxidation and Reductive Oxirane Ring-Opening Strategy

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Highly efficient synthesis of medium-sized lactones via oxidative lactonization: concise total synthesis of isolaurepan

(2009) Makoto Ebine et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

Formal Synthesis of Salinosporamide A Starting from d-Glucose

(2009) Noritaka Chida et al.   SYNTHESIS-STUTTGART

Formal synthesis of salinosporamide A via NHC-catalyzed intramolecular lactonization

(2009) Justin R. Struble et al.   TETRAHEDRON

Discovery and development of the anticancer agent salinosporamide A (NPI-0052)

(2008) William Fenical et al.   BIOORGANIC & MEDICINAL CHEMISTRY

Total Synthesis of Salinosporamide A

(2008) Takeo Fukuda et al.   ORGANIC LETTERS

Formal synthesis of salinosporamide A using a nickel-catalyzed reductive aldol cyclization–lactonization as a key step

(2008) Isabel Villanueva Margalef et al.   TETRAHEDRON

New synthetic route to access (±) salinosporamide A via an oxazolone-mediated ene-type reaction

(2008) Robert A. Mosey et al.   TETRAHEDRON LETTERS

Highly Efficient Stereocontrolled Total Synthesis of (+)-Upial

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