Loss of Chirality through Facile Lewis Base Mediated Aza-enolate Formation in Na and K (S)-N-(α-Methylbenzyl)methallylamides
Author:
Affiliation:
1. School of Chemistry, Monash University, Clayton, Melbourne, Victoria, Australia 3800
Funder
Monash University
Australian Research Council
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.6b00445
Reference32 articles.
1. Harrison-Marchand, A.; Maddaluno, J.InLithium Compounds in Organic Synthesis;Wiley-VCH Verlag GmbH & Co. KGaA:Weinheim, 2014; p297.
2. The conjugate addition of enantiomerically pure lithium amides as homochiral ammonia equivalents: scope, limitations and synthetic applications
3. The conjugate addition of enantiomerically pure lithium amides as chiral ammonia equivalents part II: 2005−2011
4. Chiral base route to functionalised cyclopentenyl amines: formal synthesis of the cyclopentene core of nucleoside Q
5. Fragmentation of 4-Sulfonylbicyclo[3.1.0]hexan-2-ones as the Key Step in the Enantioselective Synthesis of (1R)-cis-Chrysanthemic Acid Involving Desymmetrization of 3,3,6,6-Tetramethylbicyclo[3.1.0]hexane-2,4-dione
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