Hiersemann M., Nubbemeyer U. (ed.) The Claisen Rearrangement. Methods and Applications [PDF] - Все для студента
Asymmetric Carroll rearrangement of allyl α-acetamido-β-ketocarboxylates catalysed by a chiral palladium complex - Chemical Communications (RSC Publishing) DOI:10.1039/B505105C
Tsuji-Trost Reaction
Carroll rearrangement - Wikiwand
Palladium‐Catalyzed Decarboxylative Asymmetric Allylic Alkylation: Development, Mechanistic Understanding and Recent Advances - James - 2019 - Advanced Synthesis & Catalysis - Wiley Online Library
An Enantioselective CpRu-Catalyzed Carroll Rearrangement | Request PDF
Carroll Rearrangement - an overview | ScienceDirect Topics
Asymmetric Carroll rearrangement of allyl α-acetamido-β-ketocarboxylates catalysed by a chiral palladium complex - Chemical Communications (RSC Publishing) DOI:10.1039/B505105C
An unexpected acid-catalyzed decomposition reaction of cilnidipine and pranidipine to the decarboxylative bridged tricyclic products via cascade rearrangements - Org. Chem. Front. - X-MOL
Carroll Rearrangement - an overview | ScienceDirect Topics
Carroll rearrangement - Wikipedia
Organopalladium Chemistry - Palladium-catalysed nucleophilic allylic substitution of functionalised compounds
PDF] Enantio- and regioselective CpRu-catalyzed Carroll rearrangement | Semantic Scholar
Thesis Reference
Carroll rearrangement - Wikipedia
Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism | Nature Communications
Pd(OAc) 2 -catalyzed asymmetric hydrogenation of sterically hindered N -tosylimines | Nature Communications
Introduction to the Development of a Catalytic Asymmetric Synthesis of Tertiary α-Aryl Ketones | SpringerLink
Asymmetric Carroll rearrangement of allyl α-acetamido-β-ketocarboxylates catalysed by a chiral palladium complex - Chemical Communications (RSC Publishing) DOI:10.1039/B505105C
Copper(II)- and palladium(II)-catalyzed enantioselective Claisen rearrangement of allyloxy- and propargyloxy-indoles to quaternary oxindoles and spirocyclic lactones. - Abstract - Europe PMC