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ChemInform Abstract: Divergent Regioselectivity in the Synthesis of Trisubstituted Allylic Alcohols by Nickel- and Ruthenium-Catalyzed Alkyne Hydrohydroxymethylation with Formaldehyde.

✍ 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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πŸ“œ SIMILAR VOLUMES


Divergent Regioselectivity in the Synthe
✍ Dr. Cory C. Bausch; Ryan L. Patman; Prof. Bernhard Breit; Prof. Michael J. Krisc πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 304 KB πŸ‘ 2 views

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

Divergent Regioselectivity in the Synthe
✍ Dr. Cory C. Bausch; Ryan L. Patman; Prof. Bernhard Breit; Prof. Michael J. Krisc πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 315 KB πŸ‘ 2 views

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