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Literature DB >> 11592215

Synthesis of the (+)-C26-C40 Domain of the Azaspiracids by a Novel Double Intramolecular Hetero-Michael Addition Strategy This work was supported by the United States National Institute of Environmental Health Sciences (NIEHS; grant number ES10615), NIH, and by Bristol-Myers Squibb (CJF). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIEHS, NIH, or BMS. We thank Dr. A. B. Dounay and Dr. G. Florence for critical reading of the manuscript.

Craig J. Forsyth¹, Junliang Hao, Josep Aiguade.

Abstract

Entities: Chemical

Year: 2001 PMID： 11592215 DOI： 10.1002/1521-3773(20011001)40:19<3663::aid-anie3663>3.0.co;2-u

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

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9 in total

1. Synthesis of the ABCD and ABCDE ring systems of azaspiracid-1.

Authors: Xiao-Ti Zhou; Rich G Carter
Journal: Chem Commun (Camb) Date: 2004-09-20 Impact factor: 6.222

2. Synthesis of the southern FGHI ring system of azaspiracid-1 and investigation into the controlling elements of C28- and C36-ketalization.

Authors: Xiao-Ti Zhou; Liang Lu; Daniel P Furkert; Charles E Wells; Rich G Carter
Journal: Angew Chem Int Ed Engl Date: 2006-11-20 Impact factor: 15.336

3. Synthesis of the C1-C26 northern portion of azaspiracid-1: kinetic versus thermodynamic control of the formation of the bis-spiroketal.

Authors: Xiao-Ti Zhou; Rich G Carter
Journal: Angew Chem Int Ed Engl Date: 2006-03-03 Impact factor: 15.336

4. Synthetic and Computational Studies on the ABC Trioxadispiroketal Subunit of the Marine Biotoxin Azaspiracid-1.

Authors: Jialiang Li; Xiaohua Li; David R Mootoo
Journal: Nat Prod Commun Date: 2008-11 Impact factor: 0.986

5. Bisphosphine-catalyzed mixed double-Michael reactions: asymmetric synthesis of oxazolidines, thiazolidines, and pyrrolidines.

Authors: Vardhineedi Sriramurthy; Gregg A Barcan; Ohyun Kwon
Journal: J Am Chem Soc Date: 2007-10-09 Impact factor: 15.419

1. Synthesis of the ABCD and ABCDE ring systems of azaspiracid-1.

2. Synthesis of the southern FGHI ring system of azaspiracid-1 and investigation into the controlling elements of C28- and C36-ketalization.

3. Synthesis of the C1-C26 northern portion of azaspiracid-1: kinetic versus thermodynamic control of the formation of the bis-spiroketal.

4. Synthetic and Computational Studies on the ABC Trioxadispiroketal Subunit of the Marine Biotoxin Azaspiracid-1.

5. Bisphosphine-catalyzed mixed double-Michael reactions: asymmetric synthesis of oxazolidines, thiazolidines, and pyrrolidines.

6. Application of a Double Aza-Michael Reaction in a 'Click, Click, Cy-Click' Strategy: From Bench to Flow.

7. Synthesis of the ABC ring system of azaspiracid. 1. Effect of D ring truncation on bis-spirocyclization.

8. Total synthesis of (+)-azaspiracid-1. An exhibition of the intricacies of complex molecule synthesis.

9. Synthesis of the 8,19-Epoxysteroid Eurysterol A.