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Lin Guo-Qiang
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http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_34/101021ja054401w/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_20/101021ja0768892/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_17/101021ja061114z/authorship/3
http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_2/101021jo0485637/authorship/3
http://hub.abes.fr/acs/periodical/achre4/2008/volume_41/issue_7/101021ar7002623/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_17/101021ja0710914/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_8/101021jo8002979/authorship/5
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Catalytic Enantioselective Synthesis of Chiral Phthalides by SmI2-Mediated Reductive Cyclization of 2-Acylarylcarboxylates [J. Am. Chem. Soc.2006, 128,5624−5625].
Catalytic Enantioselective Synthesis of Chiral Phthalides by SmI2-MediatedReductive Cyclization of 2-Acylarylcarboxylates
A New Entry to Asymmetric Synthesis of Optically Activeα,γ-Substituted γ-Butyrolactones, Using a Carbohydrate DerivedAmide as Both a Chiral Auxiliary and a Proton Source
Concise Asymmetric Synthesis of (+)-CP-99,994and (+)-L-733,060 via Efficient Construction ofHomochiral syn-1,2-Diamines and syn-1,2-AminoAlcohols
Design of C2-Symmetric Tetrahydropentalenes as New Chiral Diene Ligandsfor Highly Enantioselective Rh-Catalyzed Arylation of N-Tosylarylimines withArylboronic Acids
A Highly Efficient and Direct Approach for Synthesis of Enantiopure β-AminoAlcohols by Reductive Cross-Coupling of Chiral N-tert-Butanesulfinyl Imineswith Aldehydes
An Advance on Exploring N-tert-Butanesulfinyl Imines in Asymmetric Synthesis of Chiral Amines
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