Regioselectivity of Vinyl Sulfone Based 1,3-Dipolar Cycloaddition Reactions with Sugar Azides by Computational and Experimental Studies-Reference-Cited by-同舟云学术

Regioselectivity of Vinyl Sulfone Based 1,3-Dipolar Cycloaddition Reactions with Sugar Azides by Computational and Experimental Studies

Published:2014-04-03 Issue:8 Volume:16 Page:2100-2103
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Sahu Debashis¹,Dey Santu²,Pathak Tanmaya²,Ganguly Bishwajit¹

Affiliation:

1. Computation and Simulation Unit, Analytical Discipline & Centralized Instrument Facility, and Academy of Scientific and Innovative Research, CSIR-Central Salt and Marine Chemicals Research Institute, Bhavnagar, Gujarat 364002, India

2. Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721 302, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol500461s

Reference40 articles.

1. Cu I ‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective

2. The growing applications of click chemistry

3. Azide–Alkyne 1,3-Dipolar Cycloadditions: a Valuable Tool in Carbohydrate Chemistry

4. Click chemistry reactions in medicinal chemistry: Applications of the 1,3-dipolar cycloaddition between azides and alkynes

5. Click Chemistry and Medicinal Chemistry: A Case of “Cyclo-Addiction”

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