Molecules | Free Full-Text | A General and Simple Diastereoselective Reduction by L-Selectride: Efficient Synthesis of Protected (4S,5S)-Dihydroxy Amides | HTML
L/N/K-Selectride | Chem-Station Int. Ed.
L-selectride - Wikipedia
Selectivity of reducing agents
L-selectride - Wikipedia
L-selectride-mediated highly diastereoselective asymmetric reductive aldol reaction: access to an important subunit for bioactive molecules. - Abstract - Europe PMC
Reduction and Oxidation :: Boron Hydrides
L-selectride | A Retrosynthetic Life
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
Aspects of stereocontrol in the L-Selectride reduction of 4-acyl-1,3-dioxolane derivatives - ScienceDirect
Red-Al | Chem-Station Int. Ed.
K-Selectride solution, 1.0 M p | 220760-100ml | SIGMA ALDRICH | SLS
L 17 Organic Synthesis#Chemistry#L&K-selectride - YouTube
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
LiAlH4, NaBH4, LiBH4, BH3, DIBAL, L Selectride: Reactions, Mechanis - YouTube
L-selectride - Wikipedia
Reduction with Metal Hydrides | Chem-Station Int. Ed.
PDF) A General and Simple Diastereoselective Reduction by L-Selectride: Efficient Synthesis of Protected (4S,5S)-Dihydroxy Amides
Reduction reactions
Chemical Reactivity
L-selectride-mediated highly diastereoselective asymmetric reductive aldol reaction: access to an important subunit for bioactive molecules. - Abstract - Europe PMC
Stereoselective syntheses of galanthamine and its stereoisomers by complementary Luche and L-selectride reductions - ScienceDirect
Aspects of stereocontrol in the L-Selectride reduction of 4-acyl-1,3-dioxolane derivatives - ScienceDirect
![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")
PDF] A General and Simple Diastereoselective Reduction by l-Selectride: Efficient Synthesis of Protected (4S,5S)-Dihydroxy Amides | Semantic Scholar
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
MCQ about K-selectride reduction: For exams like, CSIR-NET, GATE, IIT-JAM, BARC, BS-MS, B.Sc, M.Sc. - YouTube
Reduction of cyclic enone with bulky trialkylborohydrides - ScienceDirect
