ChemInform Abstract: Sc(OTf)<sub>3</sub>‐Catalyzed [3 + 3] Annulation of Cyclopropane 1,1‐Diesters with Mercaptoacetaldehyde: A Facile Strategy for the Synthesis of Tetrahydrothiopyranols.

Wang, Hua‐Peng; Zhang, Huan‐Huan; Hu, Xiu‐Qin; Xu, Peng‐Fei; Luo, Yong‐Chun

doi:10.1002/chin.201538161

ChemInform

2015

DOI: 10.1002/chin.201538161

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ChemInform Abstract: Sc(OTf)₃‐Catalyzed [3 + 3] Annulation of Cyclopropane 1,1‐Diesters with Mercaptoacetaldehyde: A Facile Strategy for the Synthesis of Tetrahydrothiopyranols.

Hua‐Peng Wang

Huan‐Huan Zhang

Xiu‐Qin Hu

et al.

Abstract: A Sc(OTf)3‐catalyzed formal [3 + 3] cycloaddition of cyclopropane dicarboxylates with mercaptoacetaldehyde is developed to produce tetrahydrothiopyranols in good yields.

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ChemInform Abstract: Sc(OTf)₃‐Catalyzed [3 + 3] Annulation of Cyclopropane 1,1‐Diesters with Mercaptoacetaldehyde: A Facile Strategy for the Synthesis of Tetrahydrothiopyranols.

Abstract: A Sc(OTf)3‐catalyzed formal [3 + 3] cycloaddition of cyclopropane dicarboxylates with mercaptoacetaldehyde is developed to produce tetrahydrothiopyranols in good yields.

Cited by 0 publications

References 1 publication

No citations

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ChemInform Abstract: Sc(OTf)3‐Catalyzed [3 + 3] Annulation of Cyclopropane 1,1‐Diesters with Mercaptoacetaldehyde: A Facile Strategy for the Synthesis of Tetrahydrothiopyranols.

Abstract: A Sc(OTf)3‐catalyzed formal [3 + 3] cycloaddition of cyclopropane dicarboxylates with mercaptoacetaldehyde is developed to produce tetrahydrothiopyranols in good yields.

Cited by 0 publications

References 1 publication

No citations

Contact Info

Product

Resources

About

ChemInform Abstract: Sc(OTf)₃‐Catalyzed [3 + 3] Annulation of Cyclopropane 1,1‐Diesters with Mercaptoacetaldehyde: A Facile Strategy for the Synthesis of Tetrahydrothiopyranols.