Total Synthesis of (−)-Spiroleucettadine-Reference-Cited by-同舟云学术

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Total Synthesis of (−)-Spiroleucettadine

Published:2017-10-20 Issue:46 Volume:56 Page:14663-14666
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Lamb Richard A.¹,Aberle Nicholas S.²³,Lucas Nigel T.¹,Lessene Guillaume²³,Hawkins Bill C.¹^ORCID

Affiliation:

1. Department of Chemistry; University of Otago; Dunedin 9054 New Zealand

2. The Walter and Eliza Hall Institute of Medical Research; 1G Royal Parade Parkville 3052 Australia

3. Department of Medical Biology and Department of Pharmacology and Therapeutics; The University of Melbourne; Parkville 3050 Australia

Funder

National Health and Medical Research Council

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference37 articles.

1. Natural products: A continuing source of novel drug leads

2. A New Structural Theme in the Imidazole-Containing Alkaloids from a Calcareous Leucetta Sponge

3. Studies directed toward the synthesis of the guanidine alkaloid, spiroleucettadine: some observations at the level of structure

4. Synthetic studies toward spiroleucettadine

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1. Ni-catalyzed enantioselective three-component reductive alkylacylation of alkenes: modular access to structurally complex α-amino ketones;Chemical Science;2024

2. Nickel‐Catalyzed Enantioselective Decarboxylative Acylation: Rapid, Modular Access to α‐Amino Ketones**;Angewandte Chemie International Edition;2023-11-16

3. Nickel‐Catalyzed Enantioselective Decarboxylative Acylation: Rapid, Modular Access to α‐Amino Ketones**;Angewandte Chemie;2023-11-16

4. Tumour cell suppression by spiroleucettadine through dual regulation of cell cycle and apoptosis;F1000Research;2022-11-16

5. Catalyst-free hierarchical reduction of CO2 with BH3N(C2H5)3 for selective N-methylation and N-formylation of amines;Journal of CO2 Utilization;2021-08

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