A Novel Regio- and Stereoselective Synthesis of Sulfamidates from 1,2-Diols Using Burgess and Related Reagents: A Facile Entry into β-Amino Alcohols We thank Professor K. Barry Sharpless for the gracious donation of several of the starting diol substrates. We also thank Drs. D. H. Huang, G. Suizdak, and R. Chadja for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, predoctoral fellowships from the National Science Foundation and Pfizer (S.A.S.), a postdoctoral fellowship from The Skaggs Institute for Chemical Biology (X.H.), and grants from American Biosciences, Amgen, Array Biopharma, Boehringer-Ingelheim, Glaxo, Hoffman-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.

Angewandte Chemie International Edition ◽

10.1002/1521-3773(20020301)41:5<834::aid-anie834>3.0.co;2-v ◽

2002 ◽

Vol 41 (5) ◽

pp. 834 ◽

Author(s):

K. C. Nicolaou ◽

Xianhai Huang ◽

Scott A. Snyder ◽

Paraselli Bheema Rao ◽

Marco Bella ◽

...

Keyword(s):

Financial Support ◽

National Science Foundation ◽

Chemical Biology ◽

Stereoselective Synthesis ◽

Amino Alcohols ◽

Mass Spectrometric ◽

X Ray ◽

National Science ◽

Postdoctoral Fellowship

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HIO3 and I2O5: Mild and Selective Alternative Reagents to IBX for the Dehydrogenation of Aldehydes and Ketones We thank Dr. D. H. Huang, Dr. G. Suizdak, and Dr. Raj Chahda for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, fellowships from GlaxoWellcome (T.M.) and the National Science Foundation (P.S.B.), and grants from Amgen, Array Biopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.

Angewandte Chemie ◽

10.1002/1521-3757(20020415)114:8<1444::aid-ange1444>3.0.co;2-t ◽

2002 ◽

Vol 114 (8) ◽

pp. 1444 ◽

Author(s):

K. C. Nicolaou ◽

Tamsyn Montagnon ◽

Phil S. Baran

Keyword(s):

Financial Support ◽

National Science Foundation ◽

Chemical Biology ◽

Mass Spectrometric ◽

X Ray ◽

National Science ◽

Aldehydes And Ketones

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Highly Enantioselective Inverse-Electron-Demand Hetero-DielsâAlder Reactions of Î±,Î²-Unsaturated Aldehydes This work was supported by the NIH (GM-59316), with additional support from the Schweizerischer Nationalfonds zur FÃ¶rderung der wissenschaftlichen Forschung (postdoctoral fellowship to K.G.), and the National Science Foundation (predoctoral fellowship to D.E.C.). We are grateful to Dr. R. Staples for carrying out the X-ray crystal structure analysis of 1.

Angewandte Chemie ◽

10.1002/1521-3757(20020816)114:16<3185::aid-ange3185>3.0.co;2-s ◽

2002 ◽

Vol 114 (16) ◽

pp. 3185 ◽

Author(s):

Karl Gademann ◽

David E. Chavez ◽

Eric N. Jacobsen

Keyword(s):

Crystal Structure ◽

Structure Analysis ◽

National Science Foundation ◽

Crystal Structure Analysis ◽

X Ray ◽

Inverse Electron Demand ◽

National Science ◽

Additional Support ◽

Postdoctoral Fellowship ◽

Electron Demand

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A Click Chemistry Approach to Tetrazoles by Huisgen 1,3-Dipolar Cycloaddition: Synthesis of 5-Acyltetrazoles from Azides and Acyl Cyanides We thank the National Institute of General Medical Sciences, National Institutes of Health (GM-28384), the National Science Foundation (CHE-9985553), the Skaggs Institute for Chemical Biology for a Predoctoral Fellowship (Z.D.), and the W. M. Keck Foundation for financial support.

Angewandte Chemie ◽

10.1002/1521-3757(20020617)114:12<2217::aid-ange2217>3.0.co;2-x ◽

2002 ◽

Vol 114 (12) ◽

pp. 2217 ◽

Author(s):

Zachary P. Demko ◽

K. Barry Sharpless

Keyword(s):

Click Chemistry ◽

Financial Support ◽

National Science Foundation ◽

Chemical Biology ◽

National Institutes Of Health ◽

Dipolar Cycloaddition ◽

Medical Sciences ◽

National Science

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A Click Chemistry Approach to Tetrazoles by Huisgen 1,3-Dipolar Cycloaddition: Synthesis of 5-Acyltetrazoles from Azides and Acyl Cyanides We thank the National Institute of General Medical Sciences, National Institutes of Health (GM-28384), the National Science Foundation (CHE-9985553), the Skaggs Institute for Chemical Biology for a Predoctoral Fellowship (Z.D.), and the W. M. Keck Foundation for financial support.

Angewandte Chemie International Edition ◽

10.1002/1521-3773(20020617)41:12<2113::aid-anie2113>3.0.co;2-q ◽

2002 ◽

Vol 41 (12) ◽

pp. 2113 ◽

Author(s):

Zachary P. Demko ◽

K. Barry Sharpless

Keyword(s):

Click Chemistry ◽

Financial Support ◽

National Science Foundation ◽

Chemical Biology ◽

National Institutes Of Health ◽

Dipolar Cycloaddition ◽

Medical Sciences ◽

National Science

Download Full-text

Highly Enantioselective Inverse-Electron-Demand Hetero-DielsâAlder Reactions of Î±,Î²-Unsaturated Aldehydes This work was supported by the NIH (GM-59316), with additional support from the Schweizerischer Nationalfonds zur FÃ¶rderung der wissenschaftlichen Forschung (postdoctoral fellowship to K.G.), and the National Science Foundation (predoctoral fellowship to D.E.C.). We are grateful to Dr. R. Staples for carrying out the X-ray crystal structure analysis of 1.

Angewandte Chemie International Edition ◽

10.1002/1521-3773(20020816)41:16<3059::aid-anie3059>3.0.co;2-i ◽

2002 ◽

Vol 41 (16) ◽

pp. 3059 ◽

Author(s):

Karl Gademann ◽

David E. Chavez ◽

Eric N. Jacobsen

Keyword(s):

Crystal Structure ◽

Structure Analysis ◽

National Science Foundation ◽

Crystal Structure Analysis ◽

X Ray ◽

Inverse Electron Demand ◽

National Science ◽

Additional Support ◽

Postdoctoral Fellowship ◽

Electron Demand

Download Full-text

A Biomimetically Inspired Synthesis of the Dehydropiperidine Domain of Thiostrepton We thank Drs. D. H. Huang and L. Pasternack, G. Suizdak, and R. Chadja for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), fellowships from The Academy of Finland (M.N.), The Skaggs Institute for Research (M.Z.), and Bayer AG (S.B.), and grants from Abbott, Amgen, Array Biopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.

Angewandte Chemie International Edition ◽

10.1002/1521-3773(20020603)41:11<1941::aid-anie1941>3.0.co;2-v ◽

2002 ◽

Vol 41 (11) ◽

pp. 1941 ◽

Author(s):

K. C. Nicolaou ◽

Marta Nevalainen ◽

Brian S. Safina ◽

Mark Zak ◽

Stephan Bulat

Keyword(s):

Financial Support ◽

Chemical Biology ◽

Mass Spectrometric ◽

National Institutes Of Health ◽

Download Full-text

A Click Chemistry Approach to Tetrazoles by Huisgen 1,3-Dipolar Cycloaddition: Synthesis of 5-Sulfonyl Tetrazoles from Azides and Sulfonyl Cyanides We thank the National Institute of General Medical Sciences, National Institutes of Health (GM-28384), the National Science Foundation (CHE-9985553), the Skaggs Institute for Chemical Biology for a Predoctoral Fellowship (Z.D.), and the W. M. Keck Foundation for financial support. Dedicated to Professor Rolf Huisgen, the pioneer of this large and extremely useful family of reactions.

Angewandte Chemie International Edition ◽

10.1002/1521-3773(20020617)41:12<2110::aid-anie2110>3.0.co;2-7 ◽

2002 ◽

Vol 41 (12) ◽

pp. 2110 ◽

Author(s):

Zachary P. Demko ◽

K. Barry Sharpless

Keyword(s):

Click Chemistry ◽

Financial Support ◽

National Science Foundation ◽

Chemical Biology ◽

National Institutes Of Health ◽

Dipolar Cycloaddition ◽

Medical Sciences ◽

National Science

Download Full-text

A Biomimetically Inspired Synthesis of the Dehydropiperidine Domain of Thiostrepton We thank Drs. D. H. Huang and L. Pasternack, G. Suizdak, and R. Chadja for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), fellowships from The Academy of Finland (M.N.), The Skaggs Institute for Research (M.Z.), and Bayer AG (S.B.), and grants from Abbott, Amgen, Array Biopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.

Angewandte Chemie ◽

10.1002/1521-3757(20020603)114:11<2021::aid-ange2021>3.0.co;2-j ◽

2002 ◽

Vol 114 (11) ◽

pp. 2021 ◽

Author(s):

K. C. Nicolaou ◽

Marta Nevalainen ◽

Brian S. Safina ◽

Mark Zak ◽

Stephan Bulat

Keyword(s):

Financial Support ◽

Chemical Biology ◽

Mass Spectrometric ◽

National Institutes Of Health ◽

Download Full-text

A Click Chemistry Approach to Tetrazoles by Huisgen 1,3-Dipolar Cycloaddition: Synthesis of 5-Sulfonyl Tetrazoles from Azides and Sulfonyl Cyanides We thank the National Institute of General Medical Sciences, National Institutes of Health (GM-28384), the National Science Foundation (CHE-9985553), the Skaggs Institute for Chemical Biology for a Predoctoral Fellowship (Z.D.), and the W. M. Keck Foundation for financial support. Dedicated to Professor Rolf Huisgen, the pioneer of this large and extremely useful family of reactions.

Angewandte Chemie ◽

10.1002/1521-3757(20020617)114:12<2214::aid-ange2214>3.0.co;2-e ◽

2002 ◽

Vol 114 (12) ◽

pp. 2214 ◽

Author(s):

Zachary P. Demko ◽

K. Barry Sharpless

Keyword(s):

Click Chemistry ◽

Financial Support ◽

National Science Foundation ◽

Chemical Biology ◽

National Institutes Of Health ◽

Dipolar Cycloaddition ◽

Medical Sciences ◽

National Science

Download Full-text

Double-Diffusive Convection: A report on an Engineering Foundation Conference

Journal of Fluid Mechanics ◽

10.1017/s0022112084000173 ◽

1984 ◽

Vol 138 ◽

pp. 405-416 ◽

Author(s):

C. F. Chen ◽

D. H. Johnson

Keyword(s):

Financial Support ◽

National Science Foundation ◽

Ad Hoc ◽

Double Diffusive Convection ◽

Santa Barbara ◽

Diffusive Convection ◽

National Science ◽

Scientists And Engineers ◽

Double Diffusive ◽

Diffusive System

Under the auspices of the Engineering Foundation, financial support of the National Science Foundation, and the cochairmanship of the authors, a conference on ‘Double-Diffusive Convection’ was held from 14–18 March 1983 in Santa Barbara. The conference attracted more than seventy scientists and engineers working in various disciplines, and 45 talks were presented. There was an ad hoc film session which ended with a demonstration of a laboratory experiment on crystallization in a double-diffusive system.

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