Chiral base route to functionalised cyclopentenyl amines: formal synthesis of the cyclopentene core of nucleoside Q
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference46 articles.
1. On the α-lithiation-rearrangement of N-toluensulfonyl aziridines: mechanistic and synthetic aspects
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3. Synthesis and reactions of cyclopentadiene monoaziridine: a concise approach to the core of agelastatin A
4. New Route to 4-Aminocyclopent-2-en-1-ols: Synthesis and Enantioselective Rearrangement of 4-Amino-substituted Cyclopentene Oxides
5. Total synthesis of optically pure nucleoside Q. Determination of absolute configuration of natural nucleoside Q
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1. An enantiodivergent synthesis of N-Boc-protected (R)- and (S)-4-amino cyclopent-2-en-1-one;Journal of Chemical Research;2021-10-29
2. Rearrangement Reactions Leading to Optically Active α,α-Disubstituted Primary Allylamines;European Journal of Organic Chemistry;2017-01-26
3. Loss of Chirality through Facile Lewis Base Mediated Aza-enolate Formation in Na and K (S)-N-(α-Methylbenzyl)methallylamides;Organometallics;2016-08-09
4. An Enantioselective Approach to 4-O-Protected-2-cyclopentene-l,4-diol Derivatives via a Rhodium-Catalyzed Redox-Isomerization Reaction;The Journal of Organic Chemistry;2015-12-09
5. Advances in the Chemistry of Chiral Lithium Amides;Lithium Compounds in Organic Synthesis;2014-03-21
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