Y
You Huang
Researcher at Nankai University
Publications - 123
Citations - 3073
You Huang is an academic researcher from Nankai University. The author has contributed to research in topics: Cascade reaction & Annulation. The author has an hindex of 31, co-authored 122 publications receiving 2637 citations.
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Morita–Baylis–Hillman adduct derivatives (MBHADs): versatile reactivity in Lewis base-promoted annulation
Peizhong Xie,You Huang +1 more
TL;DR: This tutorial review will describe Lewis base-promoted annulation reactions with MBHADs, with a special emphasis on recent work regarding diverse reactivities of MBH ADs.
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Domino Cyclization Initiated by Cross-Rauhut–Currier Reactions
Peizhong Xie,You Huang +1 more
TL;DR: The Rauhut-Currier reaction has proved itself as a promising strategy for synthesis of multifunctionalized molecules, although still being in its infancy with regard to limitations of selectivity and scope.
Journal ArticleDOI
Phosphine-catalyzed domino reaction: highly stereoselective synthesis of trans-2,3-dihydrobenzofurans from salicyl N-thiophosphinyl imines and allylic carbonates.
Peizhong Xie,You Huang,Ruyu Chen +2 more
TL;DR: A novel phosphine-catalyzed domino reaction of salicyl N-thiophosphinyl imines and allylic carbonates was developed, offering a powerful approach to the construction of a highly substituted trans-2,3-dihydrobenzofuran skeleton with high diastereoselectivity.
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Phosphine-catalyzed [4 + 2] annulation of γ-substituent allenoates: facile access to functionalized spirocyclic skeletons.
TL;DR: The first phosphine-catalyzed [4 + 2] annulation of γ-substituted allenoates with 2-arylidene-1H-indenes-1,3(2H)-diones is disclosed, offering a powerful approach to the construction of highly substituted spiro[4.5]dec-6-ene skeletons in excellent yields, and with complete regioselectivity and high diastereoselectivities.
Journal ArticleDOI
PPh3-Catalyzed Domino Reaction: A Facile Method for the Synthesis of Chroman Derivatives
TL;DR: A novel domino reaction catalyzed by triphenylphosphine was developed for synthesis of the highly functionalized chroman derivatives and the first example that the gamma-CH(3) of allenoate undergoes cyclization to form chroman derivates was reported.