Dedicated to Professor Barry M. Trost on the occasion of his 70th birthday. Trisubstituted allylic alcohols [1,2] are ubiquitous in natural products and are readily converted into diverse chiral building blocks by enantioselective epoxidation, [2a,b] cyclopropanation, [2a,c] hydrogenation, [2a,d] a
β¦ LIBER β¦
ChemInform Abstract: Divergent Regioselectivity in the Synthesis of Trisubstituted Allylic Alcohols by Nickel- and Ruthenium-Catalyzed Alkyne Hydrohydroxymethylation with Formaldehyde.
β Scribed by Cory C. Bausch; Ryan L. Patman; Berhard Breit; Michael J. Krische
- Publisher
- John Wiley and Sons
- Year
- 2011
- Weight
- 45 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0931-7597
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