Copper(I)-BINOL Catalyzed Domino Synthesis of 1,4-Benzoxathiines through C(aryl)-O Bond Formation
Joint Authors
Sekar, Govindasamy
Korupalli, Chiranjeevi
Prasad, D. J. C.
Dandapat, Arpan
Source
Organic Chemistry International
Issue
Vol. 2011, Issue 2011 (31 Dec. 2011), pp.1-7, 7 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2011-09-19
Country of Publication
Egypt
No. of Pages
7
Main Subjects
Abstract EN
1,4-benzoxathiine moieties can be synthesized by domino SN2 ring opening of epoxide with o-halothiophenols followed by the copper(I)-BINOL catalyzed Ullmann-type coupling cyclization (intramolecular C(aryl)-O bond formation) with moderate to good yields.
American Psychological Association (APA)
Korupalli, Chiranjeevi& Dandapat, Arpan& Prasad, D. J. C.& Sekar, Govindasamy. 2011. Copper(I)-BINOL Catalyzed Domino Synthesis of 1,4-Benzoxathiines through C(aryl)-O Bond Formation. Organic Chemistry International،Vol. 2011, no. 2011, pp.1-7.
https://search.emarefa.net/detail/BIM-513231
Modern Language Association (MLA)
Korupalli, Chiranjeevi…[et al.]. Copper(I)-BINOL Catalyzed Domino Synthesis of 1,4-Benzoxathiines through C(aryl)-O Bond Formation. Organic Chemistry International No. 2011 (2011), pp.1-7.
https://search.emarefa.net/detail/BIM-513231
American Medical Association (AMA)
Korupalli, Chiranjeevi& Dandapat, Arpan& Prasad, D. J. C.& Sekar, Govindasamy. Copper(I)-BINOL Catalyzed Domino Synthesis of 1,4-Benzoxathiines through C(aryl)-O Bond Formation. Organic Chemistry International. 2011. Vol. 2011, no. 2011, pp.1-7.
https://search.emarefa.net/detail/BIM-513231
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-513231
