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Xun Sun
Researcher at Fudan University
Publications - 22
Citations - 312
Xun Sun is an academic researcher from Fudan University. The author has contributed to research in topics: Catalysis & Reagent. The author has an hindex of 11, co-authored 21 publications receiving 275 citations.
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Highly efficient synthesis of enantioenriched fully-substituted spirocyclohexane oxindoles via a Michael-Michael-aldol cascade reaction
TL;DR: A highly efficient organocatalyzed Michael-Michael-aldol cascade reaction for the construction of enantioenriched spirocyclohexane oxindoles bearing six consecutive stereocenters has been achieved in good yields with excellent stereoselectivities under mild conditions.
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Two novel isoquinoline alkaloids from the seedling of Corydalis decumbens
TL;DR: Two new isoquinoline alkaloids, decumbensine (1) and decumbendine (2), together with nine known compounds including tetrahydropalmatine (3), bicuculline (4), allocryptopine (5), bulbocapine (6), protopine(7), kikemanine (8), decumbenine B (9), decengenine C (10), and muramine (11) were isolated from the seedling of Corydalis decumbsens (Thunb.) Pers
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Dual-Organocatalytic Michael/Michael/aldol Cascade Reaction for the Asymmetric Construction of Fully-substituted Cyclohexane
TL;DR: An efficient cascade reaction was developed affording fully-substituted cyclohexane bearing six contiguous stereocenters via Michael/Michael/aldol sequence, obtaining good yields, excellent diastereoselectivities, and enantioselectivity for a wide array of Michael acceptors.
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An efficient method for synthesis of bexagliflozin and its carbon-13 labeled analogue
TL;DR: A convenient method for highly diastereoselective synthesis of bexagliflozin 7a and its carbon-13 labeled analogue 7b was developed, which has the main feature is the stereoselectives reduction of 16 catalyzed by BF3·OEt2.
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A Concise Approach to N-Substituted Rhodanines through a Base-Assisted One-Pot Coupling and Cyclization Process
TL;DR: An efficient approach to obtain functionalized rhodanines was developed through a base-assisted one-pot coupling and continuous cyclization of a primary amine, carbon disulfide, and methyl (2-chloroacetyl)carbamate.