Remarkable Stereoselectivity in Intramolecular Borono-Mannich Reactions: Synthesis of Conduramines-Reference-Cited by-同舟云学术

Remarkable Stereoselectivity in Intramolecular Borono-Mannich Reactions: Synthesis of Conduramines

Published:2012-01-04 Issue:2 Volume:14 Page:544-547
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Norsikian Stéphanie¹,Soulé Jean-François¹,Cannillo Alexandre¹,Guillot Régis¹,Tran Huu Dau Marie-Elise¹,Beau Jean-Marie¹

Affiliation:

1. Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles du CNRS, Avenue de la Terrasse, F-91198 Gif-sur-Yvette, France, Université Paris Sud, Institut de Chimie Moléculaire et des Matériaux, F-91405 Orsay, France, and CNRS, F-91405 Orsay, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol203162s

Reference51 articles.

1. The boronic acid mannich reaction: A new method for the synthesis of geometrically pure allylamines

2. bPetasis, N. A.InMulticomponent Reactions;Zhu, J.; Bienaymé, H., Eds.Wiley-VCH: 2005, pp1999–1223.

3. Boronic Acids and Esters in the Petasis-Borono Mannich Multicomponent Reaction

4. Highly Stereocontrolled One-Step Synthesis of anti-β-Amino Alcohols from Organoboronic Acids, Amines, and α-Hydroxy Aldehydes

5. Catalytic Diastereoselective Petasis Reactions

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