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The Merck Bile Acid Cortisone Process: The Next-to-Last Word
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hlca.194402701231openalex-snapshot
Zur Kenntnis des Abbaues der Aminosäuren im tierischen Organismus. 4. Über den oxydativen Abbau der Aminosäuren im Gehirn
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STEROIDS DERIVED FROM BILE ACIDS
inferredcites →https://doi.org/10.1016/s0021-9258(17)41260-9openalex-snapshot
STEROIDS DERIVED FROM BILE ACIDS
inferredcites →https://doi.org/10.1016/s0021-9258(17)41396-2openalex-snapshot
PARTIAL SYNTHESIS OF COMPOUNDS RELATED TO ADRENAL CORTICAL HORMONES
inferredcites →https://doi.org/10.1016/s0021-9258(17)41401-3openalex-snapshot
STEROIDS DERIVED FROM BILE ACIDS
inferredcites →https://doi.org/10.1016/s0021-9258(18)35582-0openalex-snapshot
STEROIDS DERIVED FROM BILE ACIDS
inferredcites →https://doi.org/10.1016/s0021-9258(18)43084-0openalex-snapshot
DEGRADATION OF THE BILE ACID SIDE CHAIN
inferredcites →https://doi.org/10.1016/s0021-9258(18)56169-xopenalex-snapshot
STEROIDS DERIVED FROM BILE ACIDS
inferredcites →https://doi.org/10.1016/s0021-9258(18)56347-xopenalex-snapshot
STEROIDS DERIVED FROM BILE ACIDS
inferredcites →https://doi.org/10.1021/ja01106a023openalex-snapshot
Preparation and Properties of Some Additional Carcinogen—Protein Conjugates1
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Steroidal Sapogenins. VIII. Markogenin (22b-Spirostane-2ξ,3β-diol). A New Sapogenin Isolated from Yucca2
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inferredcites →https://doi.org/10.1021/ja01133a028openalex-snapshot
β-Dialkylaminoethyl Esters with Adrenergic Blocking Activity
inferredcites →https://doi.org/10.1021/ja01171a067openalex-snapshot
Synthesis of 5,5′-Dibromosalicil and Related Compounds
inferredcites →https://doi.org/10.1021/ja01182a534openalex-snapshot
EXCHANGE REACTION BETWEEN FERRIC AND FERROUS IONS IN PERCHLORIC ACID USING A DIFFUSION SEPARATION METHOD
inferredcites →https://doi.org/10.1021/ja01185a056openalex-snapshot
4,4'-Dichlorodibutyl Ether and its Derivatives from Tetrahydrofuran
inferredcites →https://doi.org/10.1021/jo01361a021openalex-snapshot
Formation of Dieckmann Reaction Products under Acyloin Conditions. Competition of the Two Reactions
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Meanderings of a Curious Chemist
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Wohl‐Ziegler Bromination
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Future Directions of Modern Organic Synthesis
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Decarboxylative Oxygenation via Photoredox Catalysis
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From Cortisone to Enlicitide: A Journey of Synthetic Chemistry Innovations at Merck
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Development of a Scalable Synthesis of the Small Molecule TGFβR1 Inhibitor BMS-986260
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Synthesis Optimization, Scale-Up, and Catalyst Screening Efforts toward the MGAT2 Clinical Candidate, BMS-963272
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From Metallacycle-Mediated Annulative Cross-Coupling to Steroidal Tetracycles through Intramolecular C9–C10 Bond Formation
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From an ent -Estrane, through a nat -Androstane, to the Total Synthesis of the Marine-Derived Δ 8,9 -Pregnene (+)-03219A
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Oxidative Diversification of Steroids by Nature-Inspired Scanning Glycine Mutagenesis of P450BM3 (CYP102A1)
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Recent Advances in Steroid Synthesis: A Tribute to Sir Derek Barton
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Carbonyl 1,2-transposition through triflate-mediated α-amination
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