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Literature DB >> 17694517

Acyclic stereocontrol in the Ireland-Claisen rearrangement of alpha-branched esters.

Ying-chuan Qin¹, Craig E Stivala, Armen Zakarian.

Abstract

Entities: Chemical

Year: 2007 PMID： 17694517 DOI： 10.1002/anie.200702142

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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20 in total

1. Studies toward the synthesis of maoecrystal V.

Authors: Zhenhua Gu; Armen Zakarian
Journal: Org Lett Date: 2011-01-27 Impact factor: 6.005

2. Generation of stereochemically defined tetrasubstituted enolborinates by 1,4-hydroboration of α,β-unsaturated morpholine carboxamides with (diisopinocampheyl)borane.

Authors: Christophe Allais; Andy S Tsai; Philippe Nuhant; William R Roush
Journal: Angew Chem Int Ed Engl Date: 2013-10-15 Impact factor: 15.336

3. A unique approach to aldol products for the creation of all-carbon quaternary stereocentres.

Authors: Jaya Prakash Das; Helena Chechik; Ilan Marek
Journal: Nat Chem Date: 2009-03-29 Impact factor: 24.427

Review 4. Synthesis and biology of cyclic imine toxins, an emerging class of potent, globally distributed marine toxins.

Authors: Craig E Stivala; Evelyne Benoit; Rómulo Aráoz; Denis Servent; Alexei Novikov; Jordi Molgó; Armen Zakarian
Journal: Nat Prod Rep Date: 2015-03 Impact factor: 13.423

5. Studies toward the synthesis of spirolide C: exploration into the formation of the 23-membered all-carbon macrocyclic framework.

Authors: Craig E Stivala; Zhenhua Gu; Lindsay L Smith; Armen Zakarian
Journal: Org Lett Date: 2012-01-19 Impact factor: 6.005

6. Enantioselective Construction of Acyclic Quaternary Carbon Stereocenters: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Amide Enolates.

Authors: Pavel Starkov; Jared T Moore; Douglas C Duquette; Brian M Stoltz; Ilan Marek
Journal: J Am Chem Soc Date: 2017-07-07 Impact factor: 15.419

Acyclic stereocontrol in the Ireland-Claisen rearrangement of alpha-branched esters.

1. Studies toward the synthesis of maoecrystal V.

2. Generation of stereochemically defined tetrasubstituted enolborinates by 1,4-hydroboration of α,β-unsaturated morpholine carboxamides with (diisopinocampheyl)borane.

3. A unique approach to aldol products for the creation of all-carbon quaternary stereocentres.

Review 4. Synthesis and biology of cyclic imine toxins, an emerging class of potent, globally distributed marine toxins.

5. Studies toward the synthesis of spirolide C: exploration into the formation of the 23-membered all-carbon macrocyclic framework.

6. Enantioselective Construction of Acyclic Quaternary Carbon Stereocenters: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Amide Enolates.

7. Total synthesis of pinnatoxins A and G and revision of the mode of action of pinnatoxin A.

8. Highly enantioselective direct alkylation of arylacetic acids with chiral lithium amides as traceless auxiliaries.

9. Forming all-carbon quaternary stereogenic centres in acyclic systems from alkynes.

Review 10. Axial preferences in allylation reactions via the Zimmerman-Traxler transition state.