A facile one-pot stereoselective synthesis of trisubstituted (E)-2-methylalk-2-enoic acids from unactivated Baylis–Hillman adducts and a simple access to some important insect pheromones-Reference-Cited by-同舟云学术

A facile one-pot stereoselective synthesis of trisubstituted (E)-2-methylalk-2-enoic acids from unactivated Baylis–Hillman adducts and a simple access to some important insect pheromones

Published:2006-09 Issue:37 Volume:47 Page:6615-6618
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Das Biswanath,Chowdhury Nikhil,Banerjee Joydeep,Majhi Anjoy

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Baylis, A. B.; Hillman, M. E. D. German Patent 2155113, 1972; Chem. Abstr. 1972, 77, 34174q.

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

3. Synthesis and Biological Activity of ?-Methylene-?-butyrolactones

4. ?-Methylidene- and ?-Alkylidene-?-lactams from Nonproteinogenic Amino Acids

5. Organic Reactions in Water: An Efficient Zinc-Mediated Stereoselective Synthesis of (E)- and (Z)-Trisubstituted Alkenes Using Unactivated Alkyl Halides

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