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- W4236998032 endingPage "9865" @default.
- W4236998032 startingPage "9861" @default.
- W4236998032 abstract "Abstract Catalytic addition of chiral phosphine, that is, ( R )‐ or ( S )‐SITCP, to an α‐substituted allene ester generated a zwitterionic dipole. Under optimized reaction conditions, this dipole could engage isatine‐derived N ‐Boc‐ketimines in a novel mode of [3+2] annulation reaction. Pyrrolinyl spirooxindoles are thus afforded in high yields and with excellent enantioselectivities. The unprecedented annulation reaction successfully facilitated the construction of sp 3 ‐rich and highly substituted 3,2′‐pyrrolidinyl spirooxindoles supporting many chiral centers." @default.
- W4236998032 created "2022-05-12" @default.
- W4236998032 creator A5033600382 @default.
- W4236998032 creator A5044808192 @default.
- W4236998032 creator A5046740490 @default.
- W4236998032 creator A5054222197 @default.
- W4236998032 creator A5065143464 @default.
- W4236998032 date "2016-06-27" @default.
- W4236998032 modified "2023-09-29" @default.
- W4236998032 title "Engaging Allene-Derived Zwitterions in an Unprecedented Mode of Asymmetric [3+2]-Annulation Reaction" @default.
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- W4236998032 doi "https://doi.org/10.1002/ange.201603936" @default.
- W4236998032 hasPublicationYear "2016" @default.
- W4236998032 type Work @default.