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A Novel and Affordable Process for the Synthesis of Dl-Cloprostenol Sodium for Animal Producers

https://doi.org/10.2139/ssrn.4804416
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/chir.22457openalex-extracted
An Improved and Efficient Process for the Preparation of (+)‐cloprostenol
inferredcites →https://doi.org/10.1016/0022-328x(86)80314-xopenalex-extracted
Carbanions phosphonates α-lithiés: synthèse, basicité comparée et stabilité à l'autocondensation
inferredcites →https://doi.org/10.1016/0040-4020(81)85079-xopenalex-extracted
Syntheses of PGF2α, and cloprostenol
inferredcites →https://doi.org/10.1016/s0090-6980(74)80044-4openalex-extracted
16-Aryloxyprostaglandins: A new class of potent luteolytic agent
inferredcites →https://doi.org/10.1017/s1751731112001954openalex-extracted
The roles of livestock in developing countries
inferredcites →https://doi.org/10.1021/cr00094a007openalex-extracted
The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects
inferredcites →https://doi.org/10.1021/cr60287a005openalex-extracted
Olefin synthesis with organic phosphonate carbanions
inferredcites →https://doi.org/10.1021/ja01048a062openalex-extracted
Stereo-controlled synthesis of dl-prostaglandins F2.alpha. and E2
inferredcites →https://doi.org/10.1021/ja01468a042openalex-extracted
The Utility of Phosphonate Carbanions in Olefin Synthesis
inferredcites →https://doi.org/10.1021/jm051060oopenalex-extracted
Rationally Designed Nucleoside Antibiotics That Inhibit Siderophore Biosynthesis of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1021/jo030297uopenalex-extracted
An Efficient Synthesis of an αvβ3 Antagonist
inferredcites →https://doi.org/10.1093/biolre/ioab070openalex-extracted
Cloprostenol, a synthetic analog of prostaglandin F2α induces functional regression in cultured luteal cells of felids
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