Iodine catalysis: A green alternative to transition metals in organic chemistry and technology; Resource-Efficient Technologies; Vol. 1, Iss. 1

Iodine catalysis: A green alternative to transition metals in organic chemistry and technology; Resource-Efficient Technologies; Vol. 1, Iss. 1

Opis bibliograficzny
Parent link:Resource-Efficient Technologies: electronic scientific journal/ National Research Tomsk Polytechnic University (TPU).— , 2015-.— 2405-6537
Vol. 1, Iss. 1.— 2015.— [P. 49-67]
1. autor: Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich)
Korporacja: Национальный исследовательский Томский политехнический университет (ТПУ) Институт природных ресурсов (ИПР) Кафедра технологии органических веществ и полимерных материалов (ТОВПМ)
Kolejni autorzy: Zhdankin V. V. Viktor Vladimirovich
Streszczenie:Title screen
Iodine and compounds of iodine in higher oxidation states have emerged as versatile and environmentally benign reagents for organic chemistry. One of the most impressive recent achievements in this area has been the discovery of catalytic activity of iodine in numerous oxidative transformations leading to the formation of new Csingle bondO, Csingle bondN, and Csingle bondC bonds in organic compounds. These catalytic transformations in many cases are very similar to the transition metal-catalyzed reactions, but have the advantage of environmental sustainability and efficient utilization of natural resources. Iodine is an environmentally friendly and a relatively inexpensive element, which is currently underutilized in industrial applications. One of the main goals of this review is presenting to industrial researchers the benefits of using catalytic iodine in chemical technology as an environmentally sustainable alternative to transition metals. The present review summarizes catalytic applications of iodine and compounds of iodine in organic synthesis.
Język:angielski
Wydane: 2015
Hasła przedmiotowe:
труды учёных ТПУ
электронный ресурс
катализ
йод
Dostęp online:http://earchive.tpu.ru/handle/11683/50193
Format: Elektroniczne Rozdział
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=553608

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