New C−C Coupling Reaction of Cyclic Nitronates with Carbon Nucleophiles. Umpolung of the Conventional Reactivity of Nitronates-Reference-Cited by-同舟云学术

New C−C Coupling Reaction of Cyclic Nitronates with Carbon Nucleophiles. Umpolung of the Conventional Reactivity of Nitronates

Published:2004-11-01 Issue:24 Volume:69 Page:8485-8488
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Smirnov Vladimir O.¹,Ioffe Sema L.¹,Tishkov Alexander A.¹,Khomutova Yulia A.¹,Nesterov Ivan D.¹,Antipin Michael Yu.¹,Smit William A.¹,Tartakovsky Vladimir A.¹

Affiliation:

1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Prospect 47, 119991 Moscow, Russian Federation, and A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilov Street 28, 119991 Moscow, Russian Federation %iof@ioc.ac.ru

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo048944k

Reference17 articles.

1. (a) Ono, N.TheNitro Group in Organic Synthesis; John Wiley & Sons-VCH: New York, 2001; pp 249−301.

2. (b) Torssell, K. B. G.Nitrile Oxides,Nitronesand Nitronates in Organic Synthesis; VCH: New York, 1988.

3. Prakash, S.; Schleyer, P. V. R.Stable Carbocation Chemistry; John Wiley & Sons: New York, 1997; pp 525−539 and references therein.

4. The Action of Acids on Nitronic Esters and Nitroparaffin Salts. Concerning the Mechanisms of the Nef and the Hydroxamic Acid Forming Reactions of Nitroparaffins1,2

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