Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes
The Stille-type cross coupling reaction with tetraalkynylstannanes was studied in detail for the first time. The reaction provides a simple and effective route towards a variety of arylalkynes. The advantages and limitations of the proposed procedure are discussed
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Royal Society of Chemistry
2018
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oai:10.200.131.19:20.500.12258-30402018-09-21T09:36:51Z Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes Dotsenko, V. V. Доценко, В. В. Alkyne derivative Organotin compound The Stille-type cross coupling reaction with tetraalkynylstannanes was studied in detail for the first time. The reaction provides a simple and effective route towards a variety of arylalkynes. The advantages and limitations of the proposed procedure are discussed 2018-09-21T09:36:26Z 2018-09-21T09:36:26Z 2017 Статья Levashov, A.S., Buryi, D.S., Goncharova, O.V., Konshin, V.V., Dotsenko, V.V., Andreev, A.A. Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes // New Journal of Chemistry. - 2017. - Volume 41. - Issue 8. - Pages 2910-2918 https://www.scopus.com/record/display.uri?eid=2-s2.0-85017324547&origin=resultslist&sort=plf-f&src=s&st1=Tetraalkynylstannanes+in+the+Stille+cross+&st2=&sid=97089f1e058ec08e3dec0b149bd56c66&sot=b&sdt=b&sl=57&s=TITLE-ABS-KEY%28Tetraalkynylstannanes+in+the+Stille+cross+%29&relpos=0&citeCnt=3&searchTerm= http://hdl.handle.net/20.500.12258/3040 en New Journal of Chemistry application/pdf application/pdf Royal Society of Chemistry |
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СКФУ |
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Репозиторий |
| language |
English |
| topic |
Alkyne derivative Organotin compound |
| spellingShingle |
Alkyne derivative Organotin compound Dotsenko, V. V. Доценко, В. В. Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes |
| description |
The Stille-type cross coupling reaction with tetraalkynylstannanes was studied in detail for the first time. The reaction provides a simple and effective route towards a variety of arylalkynes. The advantages and limitations of the proposed procedure are discussed |
| format |
Статья |
| author |
Dotsenko, V. V. Доценко, В. В. |
| author_facet |
Dotsenko, V. V. Доценко, В. В. |
| author_sort |
Dotsenko, V. V. |
| title |
Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes |
| title_short |
Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes |
| title_full |
Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes |
| title_fullStr |
Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes |
| title_full_unstemmed |
Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes |
| title_sort |
tetraalkynylstannanes in the stille cross coupling reaction: a new effective approach to arylalkynes |
| publisher |
Royal Society of Chemistry |
| publishDate |
2018 |
| url |
https://www.scopus.com/record/display.uri?eid=2-s2.0-85017324547&origin=resultslist&sort=plf-f&src=s&st1=Tetraalkynylstannanes+in+the+Stille+cross+&st2=&sid=97089f1e058ec08e3dec0b149bd56c66&sot=b&sdt=b&sl=57&s=TITLE-ABS-KEY%28Tetraalkynylstannanes+in+the+Stille+cross+%29&relpos=0&citeCnt=3&searchTerm= https://dspace.ncfu.ru/handle/20.500.12258/3040 |
| work_keys_str_mv |
AT dotsenkovv tetraalkynylstannanesinthestillecrosscouplingreactionaneweffectiveapproachtoarylalkynes AT docenkovv tetraalkynylstannanesinthestillecrosscouplingreactionaneweffectiveapproachtoarylalkynes |
| _version_ |
1760531734062956544 |