1,3-Dibromo-5,5-dimethylhydantoin (DBH) as a Mild and Efficient Catalyst for Chemoselective Thioacetalization of Carbonyl Compounds and Dethioacetalization Under Mild Conditions-Reference-Cited by-同舟云学术

1,3-Dibromo-5,5-dimethylhydantoin (DBH) as a Mild and Efficient Catalyst for Chemoselective Thioacetalization of Carbonyl Compounds and Dethioacetalization Under Mild Conditions

Published:2010-03-23 Issue:4 Volume:185 Page:689-696
ISSN:1042-6507
Container-title:Phosphorus, Sulfur, and Silicon and the Related Elements
language:en
Short-container-title:Phosphorus, Sulfur, and Silicon and the Related Elements

Author:

Veisi Hojat¹,Amiri Mostafa²,Hamidian Amir Hossein³,Malakootikhah Javad⁴,Fatolahi Leila⁵,Faraji Alireza²,Sedrpoushan Alireza⁶,Maleki Behrooz⁷,Saremi Shokufe Ghahri¹,Noroozi Mohammad⁸,Bahadoori Fatemeh⁹,Veisi Somayeh¹

Affiliation:

1. a Department of Chemistry , Payame Noor University (PNU) , Iran

2. b Department of Chemistry , Bu-Ali Sina University , Hamedan, Iran

3. c Department of Chemistry , University of Otago , Dunedin, New Zealand

4. d Research Center for New Technologies in Life Science Engineering , University of Tehran , Tehran, Iran

5. e Department of Chemistry , Payame Noor University (PNU) , Aleshtar, Khoramabad, Iran

6. f Chemical Industries Department , Iranian Research Organization for Science and Technology (IROST) , Tehran, Iran

7. g Department of Chemistry , Sabzevar Tarbiat Moallem University , Sabzevar, Iran

8. h Research Institute of Petroleum Industry (PIPI) , Kermanshah, Iran

9. i Science Faculty , Chemistry Department, Organic Chemistry, ITU , Istanbul, Turkey

Publisher

Informa UK Limited

Subject

Inorganic Chemistry,Organic Chemistry,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10426500902917669

Reference46 articles.

1. Protective Groups in Organic Synthesis

2. Greene , T. W. 1981. Protective Groups in Organic Synthesis, 129NewYork: John Wiley. p.

3. Chemoselective thioacetalization with odorless 2-(1,3-dithian-2-ylidene)-3-oxobutanoic acid as a 1,3-propanedithiol equivalent

4. Diastereoselectivity in the addition of grignard reagents to ketones controlled by the 1,3-dithiane 1-oxide asymmetric building block

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