3D shapes of aryl(dihydro)naphthothiophenes: a comprehensive and structural study-Reference-Cited by-同舟云学术

3D shapes of aryl(dihydro)naphthothiophenes: a comprehensive and structural study

Published:2015 Issue:44 Volume:13 Page:10844-10851
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Boufroura H.¹²³⁴,Souibgui A.¹²³⁴⁵,Gaucher A.¹²³⁴,Marrot J.¹²³⁴,Pieters G.⁶⁷⁸⁹⁴,Aloui F.⁵¹⁰¹¹¹²¹³,Ben Hassine B.⁵¹⁰¹¹¹²¹³,Clavier G.¹⁴¹⁵¹⁶¹⁷⁴,Prim D.¹²³⁴

Affiliation:

1. Université de Versailles Saint Quentin-en-Yvelines

2. Institut Lavoisier de Versailles - UMR CNRS 8180

3. 78035 Versailles Cedex

4. France

5. Faculté des Sciences de Monastir

6. CEA Saclay

7. SCBM

8. iBiTec-S

9. 91191 Gif sur Yvette

10. Laboratoire de Synthèse Organique

11. Asymétrique et Catalyse Homogène (URES56)

12. 5019 Monastir

13. Tunisia

14. ENS-Cachan

15. PPSM-UMR CNRS 853

16. Bâtiment d'Alembert

17. 94235 CACHAN Cedex

Abstract

The overall shapes of aryl(dihydro)naphthothiophenes depend on steric and electronic key parameters.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB01583A

Reference23 articles.

1. Synthesis of a Novel Chiral Binaphthyl Phospholane and Its Application in the Highly Enantioselective Hydrogenation of Enamides

2. 1,1‘-Binaphthyl Dimers, Oligomers, and Polymers: Molecular Recognition, Asymmetric Catalysis, and New Materials

3. Controlling First-Row Catalysts: Amination of Aryl and Heteroaryl Chlorides and Bromides with Primary Aliphatic Amines Catalyzed by a BINAP-Ligated Single-Component Ni(0) Complex

4. Illustrating Catalysis with Interlocking Building Blocks: A BINAP–Ruthenium Complex Catalyzed Asymmetric Hydrogenation

5. Asymmetric Conjugate Hydrocyanation of α,β-Unsaturated N-Acylpyrroles with the Ru(phgly)2(binap)–CH3OLi Catalyst System

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