Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides

No such thing as a problem substrate! In a reaction designed specifically for the title substrates C-C coupling with alkyl boranes occurred in good yield at room temperature with commercially available catalyst components (see scheme). This versatile method is also suitable for Suzuki reactions of s...

Szczegółowa specyfikacja

Opis bibliograficzny
Główni autorzy: Lu, Zhe, Fu, Gregory C.
Kolejni autorzy: Massachusetts Institute of Technology. Department of Chemistry
Format: Artykuł
Język:en_US
Wydane: Wiley Blackwell 2013
Dostęp online:http://hdl.handle.net/1721.1/82045
_version_ 1826202741663334400
author Lu, Zhe
Fu, Gregory C.
author2 Massachusetts Institute of Technology. Department of Chemistry
author_facet Massachusetts Institute of Technology. Department of Chemistry
Lu, Zhe
Fu, Gregory C.
author_sort Lu, Zhe
collection MIT
description No such thing as a problem substrate! In a reaction designed specifically for the title substrates C-C coupling with alkyl boranes occurred in good yield at room temperature with commercially available catalyst components (see scheme). This versatile method is also suitable for Suzuki reactions of secondary and primary alkyl bromides and iodides, as well as primary alkyl chlorides.
first_indexed 2024-09-23T12:15:51Z
format Article
id mit-1721.1/82045
institution Massachusetts Institute of Technology
language en_US
last_indexed 2024-09-23T12:15:51Z
publishDate 2013
publisher Wiley Blackwell
record_format dspace
spelling mit-1721.1/820452022-10-01T08:50:06Z Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides Lu, Zhe Fu, Gregory C. Massachusetts Institute of Technology. Department of Chemistry Lu, Zhe Fu, Gregory C. No such thing as a problem substrate! In a reaction designed specifically for the title substrates C-C coupling with alkyl boranes occurred in good yield at room temperature with commercially available catalyst components (see scheme). This versatile method is also suitable for Suzuki reactions of secondary and primary alkyl bromides and iodides, as well as primary alkyl chlorides. National Institute of General Medical Sciences (U.S.) (Grant R01-GM62871) Eli Lilly and Company (Fellowship) Martin Family Society of Fellows for Sustainability (Fellowship) Merck Research Laboratories Novartis (Firm) 2013-11-08T15:27:18Z 2013-11-08T15:27:18Z 2010-08 2010-05 Article http://purl.org/eprint/type/JournalArticle 14337851 1521-3773 http://hdl.handle.net/1721.1/82045 Lu, Zhe, and Gregory C. Fu. “Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides.” Angewandte Chemie International Edition 49, no. 37 (September 3, 2010): 6676-6678. en_US http://dx.doi.org/10.1002/anie.201003272 Angewandte Chemie International Edition Creative Commons Attribution-Noncommercial-Share Alike 3.0 http://creativecommons.org/licenses/by-nc-sa/3.0/ application/pdf Wiley Blackwell PMC
spellingShingle Lu, Zhe
Fu, Gregory C.
Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides
title Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides
title_full Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides
title_fullStr Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides
title_full_unstemmed Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides
title_short Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides
title_sort alkyl alkyl suzuki cross coupling of unactivated secondary alkyl chlorides
url http://hdl.handle.net/1721.1/82045
work_keys_str_mv AT luzhe alkylalkylsuzukicrosscouplingofunactivatedsecondaryalkylchlorides
AT fugregoryc alkylalkylsuzukicrosscouplingofunactivatedsecondaryalkylchlorides