“Diversity Oriented Synthesis” of Functionalized Chiral Tetrahydropyridines: Potential GABA Receptor Agonists and Azasugars from Natural Amino Acids via a Sequential Baylis−Hillman Reaction and RCM Protocol-Reference-Cited by-同舟云学术

“Diversity Oriented Synthesis” of Functionalized Chiral Tetrahydropyridines: Potential GABA Receptor Agonists and Azasugars from Natural Amino Acids via a Sequential Baylis−Hillman Reaction and RCM Protocol

Published:2008-04-15 Issue:3 Volume:10 Page:426-435
ISSN:1520-4766
Container-title:Journal of Combinatorial Chemistry
language:en
Short-container-title:J. Comb. Chem.

Author:

Krishna Palakodety Radha¹,Reddy P. Srinivas¹

Affiliation:

1. D-206/B, Discovery Laboratory, Organic Chemistry Division III, Indian Institute of Chemical Technology, Hyderabad 500 007, India

Publisher

American Chemical Society (ACS)

Subject

General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cc700171p

Reference50 articles.

1. Recent Advances in the Baylis−Hillman Reaction and Applications

2. Diversely Substituted Sugar-Linked α,β-Unsaturated γ-Lactones from Sugar-Derived Baylis−Hillman Adducts via a RCM

3. The Asymmetric Baylis−Hillman Reaction

4. An enantio- and stereocontrolled synthesis of (–)-mycestericin E via cinchona alkaloid-catalyzed asymmetric Baylis–Hillman reaction

5. Use of a Baylis–Hillman adduct in the stereoselective synthesis of syributins via a RCM protocol

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