In Grignard Reagent Formation from Cyclopropyl Bromide in Diethyl Ether, Trapping by DCPH Is Consistent with Diffusing Cyclopropyl Radical Intermediates-Reference-Cited by-同舟云学术

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In Grignard Reagent Formation from Cyclopropyl Bromide in Diethyl Ether, Trapping by DCPH Is Consistent with Diffusing Cyclopropyl Radical Intermediates

Published:2001-01-25 Issue:4 Volume:3 Page:605-606
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Garst John F.¹,Ungváry Ferenc¹

Affiliation:

1. Department of Chemistry, The University of Georgia, Athens, Georgia 30602

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol007006d

Reference23 articles.

1. Hamdouchi, C.; Walborsky, H. M. InHandbook of Grignard Reagents; Silverman, G. S., Rakita, P. E., Eds.; Dekker: New York, 1996; pp 145−218.

2. Garst, J. F.; Ungváry, F. InMechanisms of Grignard ReagentFormation; Richey, H. G., Jr., Ed.; Wiley: Chichester, 2000; pp 185−275.

3. Cyclopropanes

4. Mechanism of Grignard reagent formation. Comparisons of D-model calculations with experimental product yields

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1. Miscellaneous Reactions;Applied Organic Chemistry;2020-12-11

2. Grignard reagent formation;Coordination Chemistry Reviews;2004-04

3. The quest for chiral Grignard reagents;Chemical Society Reviews;2003

4. 6 Reaction mechanisms : Part (iii) Radical and radical ion reactions;Annu. Rep. Prog. Chem., Sect. B: Org. Chem.;2002

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