Literature DB >> 17109456

Polyol synthesis through hydrocarbon oxidation: de novo synthesis of L-galactose.

Dustin J Covell1, Nicolaas A Vermeulen, Nathan A Labenz, M Christina White.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2006        PMID： 17109456      PMCID： PMC2720791          DOI： 10.1002/anie.200603321

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


× No keyword cloud information.
  23 in total

1.  The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2 Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, a NIH Postdoctoral Fellowship to C.S.B., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the Tanabe Seiyaku Co., Ltd for financial support. Finally we thank Dr George T. Furst, Dr. Patrick J. Carroll, and Dr. Rakesh Kohli of the University of Pennsylvania Spectroscopic Service Center for assistance in securing and interpreting high-field NMR spectra, X-ray crystal structures, and mass spectra, respectively.

Authors:  Amos B. Smith III; Qiyan Lin; Victoria A. Doughty; Linghang Zhuang; Mark D. McBriar; Jeffrey K. Kerns; Christopher S. Brook; Noriaki Murase; Kiyoshi Nakayama
Journal:  Angew Chem Int Ed Engl       Date:  2001-01-05       Impact factor: 15.336

2.  A highly practical and enantioselective reagent for the allylation of aldehydes.

Authors:  Katsumi Kubota; James L Leighton
Journal:  Angew Chem Int Ed Engl       Date:  2003-02-24       Impact factor: 15.336

3.  Late-stage intermolecular CH activation for lead diversification: a highly chemoselective oxyfunctionalization of the C-9 position of potent bryostatin analogues.

Authors:  Paul A Wender; Michael K Hilinski; Alexander V W Mayweg
Journal:  Org Lett       Date:  2005-01-06       Impact factor: 6.005

4.  A stereoselective synthesis of (-)-tetrodotoxin.

Authors:  Andrew Hinman; J Du Bois
Journal:  J Am Chem Soc       Date:  2003-09-24       Impact factor: 15.419

5.  A practical oligomeric [(salen)Co] catalyst for asymmetric epoxide ring-opening reactions.

Authors:  Joseph M Ready; Eric N Jacobsen
Journal:  Angew Chem Int Ed Engl       Date:  2002-04-15       Impact factor: 15.336

6.  Remote oxidation of steroids by photolysis of attached benzophenone groups.

Authors:  R Breslow; S Baldwin; T Flechtner; P Kalicky; S Liu; W Washburn
Journal:  J Am Chem Soc       Date:  1973-05-16       Impact factor: 15.419

7.  Total synthesis of (+)-amphidinolide A. Assembly of the fragments.

Authors:  Barry M Trost; Stephen T Wrobleski; John D Chisholm; Paul E Harrington; Michael Jung
Journal:  J Am Chem Soc       Date:  2005-10-05       Impact factor: 15.419

8.  Diastereoselective synthesis of all eight l-hexoses from L-ascorbic acid.

Authors:  Ludmila Ermolenko; N André Sasaki
Journal:  J Org Chem       Date:  2006-01-20       Impact factor: 4.354

9.  Catalytic enantioselective Nozaki-Hiyama allylation reaction with tethered bis(8-quinolinolato) (TBOx) chromium complex.

Authors:  Guoyao Xia; Hisashi Yamamoto
Journal:  J Am Chem Soc       Date:  2006-03-01       Impact factor: 15.419

10.  A sulfoxide-promoted, catalytic method for the regioselective synthesis of allylic acetates from monosubstituted olefins via C-H oxidation.

Authors:  Mark S Chen; M Christina White
Journal:  J Am Chem Soc       Date:  2004-02-11       Impact factor: 15.419
View more
  19 in total

1.  syn-1,2-Amino alcohols via diastereoselective allylic C-H amination.

Authors:  Kenneth J Fraunhoffer; M Christina White
Journal:  J Am Chem Soc       Date:  2007-05-22       Impact factor: 15.419

2.  Catalytic intermolecular linear allylic C-H amination via heterobimetallic catalysis.

Authors:  Sean A Reed; M Christina White
Journal:  J Am Chem Soc       Date:  2008-02-27       Impact factor: 15.419

3.  A chiral Lewis acid strategy for enantioselective allylic C-H oxidation.

Authors:  Dustin J Covell; M Christina White
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

4.  Diversification of a β-Lactam Pharmacophore via Allylic C-H Amination: Accelerating Effect of Lewis Acid Co-Catalyst.

Authors:  Xiangbing Ben Qi; Grant T Rice; Manjinder S Lall; Mark S Plummer; M Christina White
Journal:  Tetrahedron       Date:  2010-06-26       Impact factor: 2.457

5.  On the macrocyclization of the erythromycin core: preorganization is not required.

Authors:  Erik M Stang; M Christina White
Journal:  Angew Chem Int Ed Engl       Date:  2011-01-27       Impact factor: 15.336

6.  Achmatowicz Reaction and its Application in the Syntheses of Bioactive Molecules.

Authors:  Arun K Ghosh; Margherita Brindisi
Journal:  RSC Adv       Date:  2016-11-24       Impact factor: 3.361

7.  A broadly applicable and practical oligomeric (salen) Co catalyst for enantioselective epoxide ring-opening reactions.

Authors:  David E White; Pamela M Tadross; Zhe Lu; Eric N Jacobsen
Journal:  Tetrahedron       Date:  2014-07-08       Impact factor: 2.457

8.  Terminal olefins to linear α,β-unsaturated ketones: Pd(II)/hypervalent iodine co-catalyzed Wacker oxidation-dehydrogenation.

Authors:  Marinus A Bigi; M Christina White
Journal:  J Am Chem Soc       Date:  2013-05-17       Impact factor: 15.419

9.  Oxidative Heck vinylation for the synthesis of complex dienes and polyenes.

Authors:  Jared H Delcamp; Paul E Gormisky; M Christina White
Journal:  J Am Chem Soc       Date:  2013-05-30       Impact factor: 15.419

10.  Allylic C-H amination for the preparation of syn-1,3-amino alcohol motifs.

Authors:  Grant T Rice; M Christina White
Journal:  J Am Chem Soc       Date:  2009-08-26       Impact factor: 15.419
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.