Synthesis of functionalized furo[2,3-b]pyridines via the Pd-catalyzed coupling of acetylenes to iodopyridones. Preparation of a key intermediate to a new HIV protease inhibitor L-754,394-Reference-Cited by-同舟云学术

Synthesis of functionalized furo[2,3-b]pyridines via the Pd-catalyzed coupling of acetylenes to iodopyridones. Preparation of a key intermediate to a new HIV protease inhibitor L-754,394

Published:1994-12 Issue:50 Volume:35 Page:9355-9358
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Houpis Ioannis N.,Choi W.B.,Reider P.J.,Molina Audrey,Churchill Hywyn,Lynch Joseph,Volante R.P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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3. L-735,524: an orally bioavailable human immunodeficiency virus type 1 protease inhibitor.

4. Highly diastereoselective reaction of a chiral, non-racemic amide enolate with (S)-glycidyl tosylate. Synthesis of the orally active HIV-1 protease inhibitor L-735,524

5. Palladium-catalyzed coupling of terminal alkynes with 5-(trifluoromethanesulfonyloxy)pyrimidine nucleosides

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