Single-Pot Access to Bisorganoborinates: Applications in Zweifel Olefination
Author:
Affiliation:
1. Department of Chemistry and Pharmacy, Ludwig-Maximilians-Universität München, Butenandtstraße 5-13, 81377 Munich, Germany
Funder
Verband der Chemischen Industrie
Ludwig-Maximilians-Universit?t M?nchen
Deutsche Forschungsgemeinschaft
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00493
Reference46 articles.
1. The Reactions of Diborane with Hydrocarbons1
2. A New Powerful Reducing Agent—Sodium Borohydride in the Presence of Aluminum Chloride and Other Polyvalent Metal Halides1,2
3. A NEW TECHNIQUE FOR THE CONVERSION OF OLEFINS INTO ORGANOBORANES AND RELATED ALCOHOLS
4. Hydroboration. I. The Reaction of Olefins with Sodium Borohydride-Aluminum Chloride. A Convenient Route to Organoboranes and the Anti-Markownikoff Hydration of Olefins
5. Hydroboration—a powerful synthetic tool
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