| Автор | McManus, S. P. |
| Автор | Carroll, J. T. |
| Автор | Grohse, P. M. |
| Автор | Pittman, C. U. |
| Дата выпуска | 1969 |
| Формат | application.pdf |
| Издатель | Taylor & Francis Group |
| Копирайт | Copyright Taylor and Francis Group, LLC |
| Название | 2,5,5-TRIMETHYL-2-OXAZOLINE |
| Тип | research-article |
| DOI | 10.1080/00304946909458389 |
| Print ISSN | 0885-6672 |
| Журнал | Organic Preparations and Procedures |
| Том | 1 |
| Первая страница | 235 |
| Последняя страница | 238 |
| Аффилиация | McManus, S. P.; Department of Chemistry, University of Alabama in Huntsville |
| Аффилиация | Carroll, J. T.; Department of Chemistry, University of Alabama in Huntsville |
| Аффилиация | Grohse, P. M.; Department of Chemistry, University of Alabama in Huntsville |
| Аффилиация | Pittman, C. U.; Department of Chemistry, University of Alabama |
| Выпуск | 4 |
| Библиографическая ссылка | McManus, McManus, P. and McManus, S. P. 1969. Chem. Commun., 235 Acid Catalyzed Cyclization Reactions, IV. For paper III, see |
| Библиографическая ссылка | (a) Author to whom inquiries should be addressed. (b) Acknowledgement is made for partial financial support from the Petroleum Research Fund, administered by the American Chemical Society, and from the National Aeronautics and Space Administration |
| Библиографическая ссылка | Petroleum Research Fund Undergraduate Scholar |
| Библиографическая ссылка | Pittman, C. U. Jr. and McManus, S. P. 20th Southeastern Regional Meeting. Dec. 4–7. pp.70Tallahassee, Fla: American Chemical Society. Abstracts |
| Библиографическая ссылка | Seeliger, W., Aufderhaar, E., Diepers, W., Feinauer, R., Nehring, R., Thier, W. and Hellmann, H. 1966. Angew. Chem. Internat. Edit., 5: 875 |
| Библиографическая ссылка | Wiley, R. H. and Bennett, L. L. 1949. Chem. Rev., 44: 447 |
| Библиографическая ссылка | McManus, S. P. 1969. Org. Preps, and Proc., 1: 183 |
| Библиографическая ссылка | McManus, S. P., Carroll, J. T., Grohse, P. M., Taddei, C. R. and Pittman, C. U. Jr. 20th Southeastern Regional Meeting. Dec. 4–7. pp.69Tallahassee, Fla: American Chemical Society. Abstracts in preparation for publication |
| Библиографическая ссылка | Fanta, P. E. and Deutsch, A. S. 1958. J. Org. Chem., 23: 72 |
| Библиографическая ссылка | Wehrmeister, H. L. 1965. J. Am. Chem. Soc., 30: 664 |
| Библиографическая ссылка | Talukbar, P. B. and Fanta, P. E. 1959. J. Am. Chem. Soc., 24: 526 |
| Библиографическая ссылка | Williams, J. W. and Hurd, C. D. 1940. J. Am. Chem. Soc., 5: 122 |
| Библиографическая ссылка | Obtained from Peninsular Chemresearch, Inc., and used without further purification. |
| Библиографическая ссылка | Some 2-oxazolines and most 5,6-dihydro-4H-1,3-oxazines are sensitive to hydrolysis in dilute acid. By using this work-up procedure, the product is not exposed to intermediate pH ranges and is extracted into the organic layer shortly after being neutralized. This method causes an increase in yield of at least 5% over that obtained by adding base to the acid solution |
| Библиографическая ссылка | 2-Oxazolines and similar compounds are very hygroscopic. Sodium hydroxide pellets<sup>15</sup> and sodium metal<sup>9</sup> are used to remove the water |
| Библиографическая ссылка | Meyers, A. I. 1960. J. Org. Chem., 25: 145 |
| Библиографическая ссылка | Litt, T. G. and BassiriLevy, A.M. 1967. Polymer Letters, 5: 871 Cyclic imino ethers polymerize fairly readily and should be stored in a clean container in a cold place; c.f |
