Chemo-enzymatic synthesis of spiro type gem-difluorocyclopropane as core molecule candidate for liquid crystal compounds-Reference-Cited by-同舟云学术

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Chemo-enzymatic synthesis of spiro type gem-difluorocyclopropane as core molecule candidate for liquid crystal compounds

Published:2009-12 Issue:12 Volume:130 Page:1157-1163
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Itoh Toshiyuki,Kanbara Manabu,Nakajima Shino,Sakuta Yusuke,Hayase Shuichi,Kawatsura Motoi,Kato Takashi,Miyazawa Kazutoshi,Uno Hidemitsu

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Environmental Chemistry,Biochemistry

Reference38 articles.

1. For a review see: A. de Meijere (Ed.), Cyclopropanes and Related Rings, Chem. Rev. 103 (2003) 931–1648.

2. Reviews see:

3. Fluorine in Bioorganic and Medicinal Chemistry,2009

4. Organofluorine Chemistry;Uneyama,2006

5. Fluorine-Containing Synthons, ACS Symposium Series 911,2005

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Experimental and Theoretical Studies on Stereomutation Through gem‐Difluorocyclopropanylide Intermediates;Asian Journal of Organic Chemistry;2024-01-15

2. Synthesis of Selectively gem‐Difluorinated Molecules; Chiral gem‐Difluorocyclopropanes via Chemo‐Enzymatic Reaction and gem‐Difluorinated Compounds via Radical Reaction;The Chemical Record;2023-03-22

3. Enantioselective Formation of All-Carbon Quaternary Stereocenters in gem-Difluorinated Cyclopropanes via Rhodium-Catalyzed Stereoablative Kinetic Resolution;Organic Letters;2022-08-11

4. Copper‐Catalyzed Enantioselective Hydrosilylation of gem ‐Difluorocyclopropenes Leading to a Stereochemical Study of the Silylated gem ‐Difluorocyclopropanes;Chemistry – A European Journal;2022-05-02

5. Asymmetric Transfer Hydrogenation of gem ‐Difluorocyclopropenyl Esters: Access to Enantioenriched gem ‐Difluorocyclopropanes;Angewandte Chemie International Edition;2020-08-25

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