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Standardization Protocols and Optimized Precursor Sets for the Efficient Application of Automated Parallel Synthesis to Lead Optimization: A Mitsunobu Example
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Steric Effects in Drug Design.
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Mitsunobu reaction modifications allowing product isolation without chromatography: application to a small parallel library
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Use of Structure−Activity Data To Compare Structure-Based Clustering Methods and Descriptors for Use in Compound Selection
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Selecting Optimally Diverse Compounds from Structure Databases: A Validation Study of Two-Dimensional and Three-Dimensional Molecular Descriptors
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Predicting Human Oral Bioavailability of a Compound: Development of a Novel Quantitative Structure-Bioavailability Relationship
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Drug Development: The role of innovation in drug development
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The mechanism of the Mitsunobu reaction. A 31P N.M.R. study
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PROGRESS IN THE MITSUNOBU REACTION. A REVIEW
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Stereospecific and Stereoselective Reactions. V. Alkylation of Active Methylene Compounds by the Use of Alcohols, Diethyl Azodicarboxylate, and Triphenylphosphine
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An Efficient Synthesis of Hindered Alkyl and Aryl Neopentyl Ethers.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Separation‐Friendly Mitsunobu Reactions: A Microcosm of Recent Developments in Separation Strategies
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Standardization Protocols and Optimized Precursor Sets for the Efficient Application of Automated Parallel Synthesis to Lead Optimization: A Mitsunobu Example.
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Metal‐Free I2‐Catalyzed Highly Selective Dehydrogenative Coupling of Alcohols and Cyclohexenones
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