Efficient tin hydride-mediated radical cyclisation of secondary amides leading to substituted pyrrolidinones. Part 2. Application to the synthesis of aromatic kainic acid analogues-Reference-Cited by-同舟云学术

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Efficient tin hydride-mediated radical cyclisation of secondary amides leading to substituted pyrrolidinones. Part 2. Application to the synthesis of aromatic kainic acid analogues

Published:1999 Issue:20 Volume: Page:2905-2910
ISSN:0300-922X
Container-title:Journal of the Chemical Society, Perkin Transactions 1
language:
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Bryans Justin S.,Large Jonathan M.,Parsons Andrew F.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1999/P1/A905809E

Cited by 27 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. Oxidative Difluoromethylation of Tetrahydroisoquinolines Using TMSCF2SPh: Synthesis of Fluorinated Pyrrolo[2,1-a]isoquinolines and Benzo[a]quinolizidines;The Journal of Organic Chemistry;2018-01-05

2. The use of J-coupling as a sole criterion to assign the total absolute stereochemistry of new pyrrolidinone class synthetic analogs, derived from S -pyroglutamic acid;Journal of Molecular Structure;2017-02

3. A Unified Strategy for Kainoid Synthesis;European Journal of Organic Chemistry;2014-06-23

4. Asymmetric Synthesis of gem-Difluoromethylenated Dihydroxypyrrolizidines and Indolizidines;The Journal of Organic Chemistry;2012-09-24

5. Bond Rotation Dynamics of Enamides: The Effect of the Acyl Group and Potential for Chirality Transfer during 5-Endo Trig Radical Cyclizations;The Journal of Organic Chemistry;2011-05-05

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