![PDF] A General and Simple Diastereoselective Reduction by l-Selectride: Efficient Synthesis of Protected (4S,5S)-Dihydroxy Amides | Semantic Scholar PDF] A General and Simple Diastereoselective Reduction by l-Selectride: Efficient Synthesis of Protected (4S,5S)-Dihydroxy Amides | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/087e7f6d7a3505c3d28e2af3fe8dac1a991c50c9/4-Figure2-1.png)
PDF] A General and Simple Diastereoselective Reduction by l-Selectride: Efficient Synthesis of Protected (4S,5S)-Dihydroxy Amides | Semantic Scholar
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Metal‐Free Reductive Aldol Reactions - Dutta - 2021 - Asian Journal of Organic Chemistry - Wiley Online Library
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L-selectride-mediated highly diastereoselective asymmetric reductive aldol reaction: access to an important subunit for bioactive molecules. - Abstract - Europe PMC
![SOLVED:Lithium tri-sec-butylborohydride, also known as L-selectride, is a metal hydride reagent that contains three sec-butyl groups bonded to boron. When this reagent is used to reduce cyclic ketones, one stereoisomer often predominates SOLVED:Lithium tri-sec-butylborohydride, also known as L-selectride, is a metal hydride reagent that contains three sec-butyl groups bonded to boron. When this reagent is used to reduce cyclic ketones, one stereoisomer often predominates](https://cdn.numerade.com/previews/63237743-c509-4d67-b785-19ca85b1acf2_large.jpg)
SOLVED:Lithium tri-sec-butylborohydride, also known as L-selectride, is a metal hydride reagent that contains three sec-butyl groups bonded to boron. When this reagent is used to reduce cyclic ketones, one stereoisomer often predominates
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L-selectride-mediated highly diastereoselective asymmetric reductive aldol reaction: access to an important subunit for bioactive molecules. - Abstract - Europe PMC
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Stereoselective syntheses of galanthamine and its stereoisomers by complementary Luche and L-selectride reductions - ScienceDirect
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MCQ about K-selectride reduction: For exams like, CSIR-NET, GATE, IIT-JAM, BARC, BS-MS, B.Sc, M.Sc. - YouTube
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The control of remote asymmetric centres via reduction of acyclic carbonyl functions - Journal of the Chemical Society, Perkin Transactions 1 (RSC Publishing) DOI:10.1039/B000155O
![PDF) A General and Simple Diastereoselective Reduction by L-Selectride: Efficient Synthesis of Protected (4S,5S)-Dihydroxy Amides PDF) A General and Simple Diastereoselective Reduction by L-Selectride: Efficient Synthesis of Protected (4S,5S)-Dihydroxy Amides](https://www.researchgate.net/publication/43352089/figure/fig1/AS:667209818992642@1536086625026/A-plausible-Cram-chelation-controlled-pathway-for-the-syn-diastereoselective-formation-of_Q320.jpg)
PDF) A General and Simple Diastereoselective Reduction by L-Selectride: Efficient Synthesis of Protected (4S,5S)-Dihydroxy Amides
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