Probing the Stereoselectivity of the Heck Arylation of Endocyclic Enecarbamates with Diazonium Salts. Concise Syntheses of (2S,5R)-Phenylproline Methyl Ester and Schramm's C-Azanucleoside-Reference-Cited by-同舟云学术

Probing the Stereoselectivity of the Heck Arylation of Endocyclic Enecarbamates with Diazonium Salts. Concise Syntheses of (2S,5R)-Phenylproline Methyl Ester and Schramm's C-Azanucleoside

Published:2003-01-10 Issue:3 Volume:5 Page:305-308
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Severino Elias A.¹,Costenaro Edson R.¹,Garcia Ariel L. L.¹,Correia Carlos Roque D.¹

Affiliation:

1. Instituto de Química, Universidade Estadual de Campinas, C. P. 6154, 13084-971, Campinas, SP, Brazil

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol027268a

Reference22 articles.

1. Advances in the Heck chemistry of aryl bromides and chlorides

2. Palladium−Imidazolium Carbene Catalyzed Mizoroki−Heck Coupling with Aryl Diazonium Ions

3. Application of a new combination of palladium and CaCO3 for an aerobic Heck reaction using arenediazonium-salts

4. Heck reaction of endocyclic enecarbamates with diazonium salts. Formal enantioselective syntheses of alkaloids (−)-codonopsine and (−)-codonopsinine, and the synthesis of a new C-aryl azasugar

5. An expeditious synthesis of 4-aryl-γ-butyrolactones, -furan-2(5H)-ones and -5-alkoxyfuran-2(5H)-ones via Heck-reaction of arenediazonium salts with 2,5-dihydrofuran

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