Literature DB >> 18062671

Solid-supported nitroso hetero diels-alder reactions. 2. Arylnitroso dienophiles: scope and limitations.

Viktor Krchnák1, Ute Moellmann, Hans-Martin Dahse, Marvin J Miller.   

Abstract

Immobilized arylnitroso dienophiles were prepared and used in hetero Diels-Alder (HDA) reactions with a variety of dienes. Polymer-supported arylnitroso species were prepared on several linkers cleavable by different cleavage reagents and used for (i) optimization of reaction conditions for HDA reactions, (ii) evaluation of the reaction outcome with various dienes, (iii) comparison of relative reactivities of dienes, and (iv) assessment of the stability of HDA adducts toward cleavage conditions typically used in solid-phase preparation (TFA). The outcome of the HDA reactions has been evaluated for a set of 19 dienes, and the relative reactivities of dienes that yielded the expected HDA adducts were compared. Cleaved products were submitted to biological assays, and the results are reported.

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Year:  2007        PMID: 18062671     DOI: 10.1021/cc7001414

Source DB:  PubMed          Journal:  J Comb Chem        ISSN: 1520-4766


  9 in total

1.  Selective molecular sequestration with concurrent natural product functionalization and derivatization: from crude natural product extracts to a single natural product derivative in one step.

Authors:  Viktor Krchňák; Jaroslav Zajíček; Patricia A Miller; Marvin J Miller
Journal:  J Org Chem       Date:  2011-11-16       Impact factor: 4.354

Review 2.  Nitroso Diels-Alder (NDA) reaction as an efficient tool for the functionalization of diene-containing natural products.

Authors:  Serena Carosso; Marvin J Miller
Journal:  Org Biomol Chem       Date:  2014-10-14       Impact factor: 3.876

Review 3.  The nitrosocarbonyl hetero-Diels-Alder reaction as a useful tool for organic syntheses.

Authors:  Brian S Bodnar; Marvin J Miller
Journal:  Angew Chem Int Ed Engl       Date:  2011-04-21       Impact factor: 15.336

4.  Iminonitroso ene reactions: experimental studies on reactivity, regioselectivity and enantioselectivity.

Authors:  Baiyuan Yang; Marvin J Miller
Journal:  Tetrahedron Lett       Date:  2010-01-13       Impact factor: 2.415

5.  Syntheses of new spirocarbocyclic nucleoside analogs using iminonitroso Diels-Alder reactions.

Authors:  Weimin Lin; Anuradha Gupta; Kyung Hee Kim; David Mendel; Marvin J Miller
Journal:  Org Lett       Date:  2009-01-15       Impact factor: 6.005

Review 6.  Chemo- and site-selective derivatizations of natural products enabling biological studies.

Authors:  Omar Robles; Daniel Romo
Journal:  Nat Prod Rep       Date:  2014-03       Impact factor: 13.423

7.  Retro iminonitroso Diels-Alder reactions: interconversion of nitroso cycloadducts.

Authors:  Baiyuan Yang; Weimin Lin; Viktor Krchnak; Marvin J Miller
Journal:  Tetrahedron Lett       Date:  2009-10-01       Impact factor: 2.415

Review 8.  Stereo- and regioselectivity of the hetero-Diels-Alder reaction of nitroso derivatives with conjugated dienes.

Authors:  Lucie Brulíková; Aidan Harrison; Marvin J Miller; Jan Hlaváč
Journal:  Beilstein J Org Chem       Date:  2016-09-01       Impact factor: 2.883

9.  Solid-Phase Synthesis of ɤ-Lactone and 1,2-Oxazine Derivatives and Their Efficient Chiral Analysis.

Authors:  Sona Krupkova; Gonzalo Pazos Aguete; Leona Kocmanova; Tereza Volna; Martin Grepl; Lucie Novakova; Marvin John Miller; Jan Hlavac
Journal:  PLoS One       Date:  2016-11-28       Impact factor: 3.240

  9 in total

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