ChemInformVolume 35, Issue 42 Isocyclic Compounds Photoinitiated Reaction of Carboxylic Acids with Oxiranes. V. V. Shevchenko, V. V. Shevchenko Inst. Macromol. Chem., Natl. Acad. Sci., Kiev 253660, UkraineSearch for more papers by this authorV. E. Pashinnik, V. E. Pashinnik Inst. Macromol. Chem., Natl. Acad. Sci., Kiev 253660, UkraineSearch for more papers by this authorO. P. Batog, O. P. Batog Inst. Macromol. Chem., Natl. Acad. Sci., Kiev 253660, UkraineSearch for more papers by this authorP. A. Bondarenko, P. A. Bondarenko Inst. Macromol. Chem., Natl. Acad. Sci., Kiev 253660, UkraineSearch for more papers by this author V. V. Shevchenko, V. V. Shevchenko Inst. Macromol. Chem., Natl. Acad. Sci., Kiev 253660, UkraineSearch for more papers by this authorV. E. Pashinnik, V. E. Pashinnik Inst. Macromol. Chem., Natl. Acad. Sci., Kiev 253660, UkraineSearch for more papers by this authorO. P. Batog, O. P. Batog Inst. Macromol. Chem., Natl. Acad. Sci., Kiev 253660, UkraineSearch for more papers by this authorP. A. Bondarenko, P. A. Bondarenko Inst. Macromol. Chem., Natl. Acad. Sci., Kiev 253660, UkraineSearch for more papers by this author First published: 27 September 2004 https://doi.org/10.1002/chin.200442091Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article. Volume35, Issue42October 19, 2004 RelatedInformation
Data are summarized on the methods of synthesis of polyfluoroalkoxysulfur trifluorides and polyfluoroalkoxy(dialkylamino)sulfur difluorides which are intermediate products in fluorination of alcohols with sulfur tetrafluoride and dialkylaminosulfur trifluoride. Their thermal and chemical transformations are also discussed.
ChemInformVolume 21, Issue 40 Reviews ChemInform Abstract: Fluorination of Organic Compounds with Fluorosulfuranes L. N. MARKOVSKII, L. N. MARKOVSKII Edited by German, L. S.; Zemskov, S. V.; Springer, D-1000 BerlinSearch for more papers by this authorV. E. PASHINNIK, V. E. PASHINNIK Edited by German, L. S.; Zemskov, S. V.; Springer, D-1000 BerlinSearch for more papers by this author L. N. MARKOVSKII, L. N. MARKOVSKII Edited by German, L. S.; Zemskov, S. V.; Springer, D-1000 BerlinSearch for more papers by this authorV. E. PASHINNIK, V. E. PASHINNIK Edited by German, L. S.; Zemskov, S. V.; Springer, D-1000 BerlinSearch for more papers by this author First published: October 2, 1990 https://doi.org/10.1002/chin.199040349Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Volume21, Issue40October 2, 1990 RelatedInformation
It has been established that the fluorination of 3β-hydroxy-Δ5,7-steroids, unlike that of 3β-hydroxy-Δ5-steroids, does not lead to the formation of 3β-fluoro derivatives. The reaction products are 3α,5α-cyclo-Δ6,8(14) compounds. Consequently, to obtain the 3β-fluoro derivatives of provitamins D — 7-dehydrocholesterol and ergosterol — the 5,7-diene system was first protected by the formation of a cyclo-adduct with 4-phenyl-1,2,4-triazoline-3,5-dione after which the adduct was fluorinated with morpholinosulfur trifluoride to the 3β-fluoro adduct, and then the 5,7-double bonds were regenerated by treating the adduct with a solution of sodium methanolate in methanol.