Tributyltin hydride-mediated cyclisations of cinnamic enamides to piperidin-2-ones or pyrrolidin-2-ones. Indolizidinone ring formation by tandem radical cyclisation-Reference-Cited by-同舟云学术

Tributyltin hydride-mediated cyclisations of cinnamic enamides to piperidin-2-ones or pyrrolidin-2-ones. Indolizidinone ring formation by tandem radical cyclisation

Published:2004-09 Issue:37 Volume:60 Page:8181-8188
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Flisińska-Łuczak Joanna,Leśniak Stanisław,Nazarski Ryszard B.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. Bowman, W. R.; Fletcher, A. J.; Potts, G. B. S. J. Chem. Soc., Perkin Trans. 1 2002, 2747–2762, and references cited therein.

2. Tributyltin hydride-induced O-stannyl ketyls in the cyclization of aldehydes and ketones with alkenes

3. Free radical cyclizations promoted by allylic O-stannyl ketyls: the intramolecular coupling of the .beta.-carbons of activated alkenes

4. Cyclization Reactions of Allylic O-Stannyl Ketyls

5. Tandem radical cyclizations promoted by O-stannyl ketyls

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Castagnoli‐Cushman Reaction of 3‐Aryl Glutaric Acids: A Convenient, Diastereoselective Reaction for 6‐Oxo‐2,4‐diarylpiperidine‐3‐carboxylic Acid Scaffold;ChemistrySelect;2022-01-21

2. Summary of DFT calculations coupled with current statistical and/or artificial neural network (ANN) methods to assist experimental NMR data in identifying diastereomeric structures;Tetrahedron Letters;2021-05

3. Unexpected Rearrangement of Dilithiated Isoindoline-1,3-diols into 3-Aminoindan-1-ones via N-Lithioaminoarylcarbenes: A Combined Synthetic and Computational Study;The Journal of Organic Chemistry;2019-08-26

4. An Eco-Friendly Stereoselective Synthesis of Novel Derivatives of Indeno[1,2-b]Pyrrole and Indeno[1,2-c]Pyridazine;Polycyclic Aromatic Compounds;2019-04-17

5. Tandem approaches for the synthesis of functionalized pyrrolidones: efficient routes toward allokainic acid and kainic acid;Tetrahedron Letters;2013-01