Efficient preparation of trisubstituted alkenes using the Julia-Lythgoe olefination of ketones. On the key-role of SmI2 in the reductive elimination step-Reference-Cited by-同舟云学术

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Efficient preparation of trisubstituted alkenes using the Julia-Lythgoe olefination of ketones. On the key-role of SmI2 in the reductive elimination step

Published:1996-03 Issue:12 Volume:37 Page:2089-2092
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Markó István E,Murphy Fiona,Dolan Simon

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. Syntheses a l'aide de sulfones v(+)- methode de synthese generale de doubles liaisons.

2. Total synthesis of (+)-milbemycin .beta.3

3. Use of Samarium Diiodide as an Alternative to Sodium/Mercury Amalgam in the Julia-Lythgoe Olefination

4. Organic chemistry with lanthanides

Cited by 52 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. An Overview of Julia-lythgoe Olefination;Current Organic Synthesis;2024-03

2. Hydroxyl-Directed Regio- and Diastereoselective Allylic Sulfone Reductions with [Sm(H₂O)_n]I₂;The Journal of Organic Chemistry;2023-12-13

3. The Sulfinylsulfonation of alkynes for β‐Sulfinyl alkenylsulfone;Chemistry – An Asian Journal;2022-05-18

4. Regio- and Diastereoselective Samarium-Mediated Allylic Benzoate Reductions;Synlett;2017-07-20

5. Metal-free, regio- and stereoselective S-methylation/phenylation of allyl halides using sulfoxides as sulfenylating agent;Tetrahedron;2017-07

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