Synthesis and Characterization of Tricarbastannatranes and Their Reactivity in B(C6F5)3-Promoted Conjugate Additions-Reference-Cited by-同舟云学术

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Synthesis and Characterization of Tricarbastannatranes and Their Reactivity in B(C6F5)3-Promoted Conjugate Additions

Published:2015-03-05 Issue:18 Volume:127 Page:5578-5582
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Kavoosi Azadeh,Fillion Eric

Funder

Natural Sciences and Engineering Research Council of Canada (NSERC)

Canadian Foundation for Innovation (CFI)

Ontario Innovation Trust (OIT)

University of Waterloo

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201500983/fullpdf

Reference28 articles.

1. NMR investigations on Stannabicycloundecanes of the type RSn(CH2CH2CH2)3N

2. e-EROS 2013

3. Stereoretentive Pd-catalysed Stille cross-coupling reactions of secondary alkyl azastannatranes and aryl halides

4. Stille Coupling of an Aziridinyl Stannatrane

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1. Synthesis and Catalytic Activity of Atrane‐type Hard and Soft Lewis Superacids with a Silyl, Germyl, or Stannyl Cationic Center;Chemistry – An Asian Journal;2021-09-06

2. Stereospecific Electrophilic Fluorination of Alkylcarbastannatrane Reagents;Angewandte Chemie International Edition;2017-09-04

3. Stereospecific Electrophilic Fluorination of Alkylcarbastannatrane Reagents;Angewandte Chemie;2017-09-04

4. Stereospecific Palladium‐Catalyzed Acylation of Enantioenriched Alkylcarbastannatranes: A General Alternative to Asymmetric Enolate Reactions;Angewandte Chemie International Edition;2016-12-16

5. Stereospecific Palladium‐Catalyzed Acylation of Enantioenriched Alkylcarbastannatranes: A General Alternative to Asymmetric Enolate Reactions;Angewandte Chemie;2016-12-16

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