Generation, structure and reactivity of tertiary organolithium reagents-Reference-Cited by-同舟云学术

Generation, structure and reactivity of tertiary organolithium reagents

Published:2015 Issue:4 Volume:32 Page:517-533
ISSN:0265-0568
Container-title:Natural Product Reports
language:en
Short-container-title:Nat. Prod. Rep.

Author:

Perry Matthew A.¹²³,Rychnovsky Scott D.⁴⁵⁶³

Affiliation:

1. Anacor Pharmaceuticals, Inc.

2. Palo Alto

3. USA

4. Department of Chemistry

5. University of California

6. Irvine

Abstract

Tertiary organolithium reagents have great potential in natural product synthesis. Recent progress in organolithium generation has made them accessible. Their utility and stereoselectivity in synthesis is discussed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/NP/C4NP00125G

Reference127 articles.

1. M. Schlosser , in Organometallics in Synthesis: A Manual, ed. M. Schlosser, John Wiley & Sons, Inc., Hoboken, NJ, USA, 2nd edn, ch. 1, pp. 1–352

2. Methods of Preparation of Organometallic Compounds.

3. Stannylation/destannylation. Preparation of .alpha.-alkoxy organolithium reagents and synthesis of dendrolasin via a carbinyl carbanion equivalent

4. Doppelt metalliertes Methanol. Alkohol‐d 1 ‐ und ‐d 3 ‐Reagenzien

Cited by 24 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. Tuning Reactivities of tert‐Butyllithium by the Addition of Stoichiometric Amounts of Tetrahydrofuran;Chemistry – A European Journal;2024-01-22

2. Continuous synthesis of 1‐ethoxy ‐2,3‐difluoro‐4‐iodo‐benzene in a microreactor system and the Gaussian and computational fluid dynamics simulations;AIChE Journal;2021-02-06

3. Trapping of Transient Organolithium Compounds;Asian Journal of Organic Chemistry;2020-08-18

4. Programmable Synthesis of 2-Deoxyglycosides;Journal of the American Chemical Society;2019-05-06

5. Preparation of Optically Enriched Secondary Alkyllithium and Alkylcopper Reagents-Synthesis of (−)-Lardolure and Siphonarienal;Angewandte Chemie International Edition;2018-03-30