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- W4310082942 abstract "We herein disclose a mild and efficient access to chiral 3-azabicyclo[3.1.0]hexanes via a Pd-catalyzed asymmetric 5-exo-trig cyclization/cyclopropanation/carbonylation of 1,6-enynes. Various nucleophiles, such as alcohols, phenols, amines and water, are well compatible with the reaction system. This reaction forms three C-C bonds, two rings, two adjacent quaternary carbon stereocenters as well as one C-O/C-N bond with excellent regio- and enantioselectivities. The products could be further functionalized to generate a library of 3-azabicyclo[3.1.0]hexane frameworks." @default.
- W4310082942 created "2022-11-30" @default.
- W4310082942 creator A5011404596 @default.
- W4310082942 creator A5025427343 @default.
- W4310082942 creator A5030890890 @default.
- W4310082942 creator A5036884020 @default.
- W4310082942 creator A5052874928 @default.
- W4310082942 creator A5076091695 @default.
- W4310082942 creator A5080592369 @default.
- W4310082942 date "2022-12-15" @default.
- W4310082942 modified "2023-09-29" @default.
- W4310082942 title "Pd‐Catalyzed Asymmetric 5‐exo‐trig Cyclization/Cyclopropanation/Carbonylation of 1,6‐Enynes for the Construction of Chiral 3‐Azabicyclo[3.1.0]hexanes" @default.
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