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Academic Journal

Diastereoselective alkylations of oxazolidinone glycolates: a useful extension of the Evans asymmetric alkylation.

  • Authors : Crimmins MT; Venable and Kenan Laboratories of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3290, USA. ; Emmitte KA

Subjects: Glycolates/Glycolates/Glycolates/*chemistry ; Oxazoles/Oxazoles/Oxazoles/*chemical synthesis; Alkylation

  • Source: Organic letters [Org Lett] 2000 Jul 13; Vol. 2 (14), pp. 2165-7.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

A practical synthesis of (S)-2-cyclohexyl-2-phenylglycolic acid via organocatalytic asymmetric construction of a tetrasubstituted carbon center.

  • Authors : Tokuda O; Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Japan.; Kano T

Subjects: Carbon/Carbon/Carbon/*chemistry ; Cyclohexanes/Cyclohexanes/Cyclohexanes/*chemical synthesis ; Glycolates/Glycolates/Glycolates/*chemical synthesis

  • Source: Organic letters [Org Lett] 2005 Oct 27; Vol. 7 (22), pp. 5103-5.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Phase-transfer-catalyzed asymmetric glycolate alkylation.

  • Authors : Andrus MB; Brigham Young University, Department of Chemistry and Biochemistry, C100 BNSN, Provo, Utah 84602-5700, USA. ; Hicken EJ

Subjects: Acetophenones* ; Cinchona Alkaloids*; Glycolates/Glycolates/Glycolates/*chemistry

  • Source: Organic letters [Org Lett] 2004 Jun 24; Vol. 6 (13), pp. 2289-92.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Synthesis of gamma,delta-unsaturated glycolic acids via sequenced brook and Ireland--claisen rearrangements.

  • Authors : Schmitt DC; Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3290, USA.; Johnson JS

Subjects: Glycolates/Glycolates/Glycolates/*chemical synthesis ; Glycolates/Glycolates/Glycolates/*chemistry; Dimerization

  • Source: Organic letters [Org Lett] 2010 Mar 05; Vol. 12 (5), pp. 944-7.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Tandem Wittig rearrangement/aldol reactions for the synthesis of glycolate aldols.

  • Authors : Bertrand MB; Department of Chemistry, University of Michigan, 930 North University Avenue, Ann Arbor, Michigan 48109-1055, USA.; Wolfe JP

Subjects: Aldehydes/Aldehydes/Aldehydes/*chemical synthesis ; Glycolates/Glycolates/Glycolates/*chemistry

  • Source: Organic letters [Org Lett] 2006 Sep 28; Vol. 8 (20), pp. 4661-3.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Synthesis and use of alpha-silyl-substituted alpha-hydroxyacetic acids.

  • Authors : Bolm C; Institute of Organic Chemistry, RWTH Aachen, Professor-Pirlet-Str. 1, D-52056 Aachen, Germany. ; Kasyan A

Subjects: Glycolates/Glycolates/Glycolates/*chemical synthesis; Biological Factors/Biological Factors/Biological Factors/chemical synthesis ; Catalysis

  • Source: Organic letters [Org Lett] 2002 Jun 27; Vol. 4 (13), pp. 2265-7.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Anti-selective glycolate aldol additions with an oxapyrone boron enolate.

  • Authors : Andrus MB; Department of Chemistry and Biochemistry, C100 BNSN, Brigham Young University, Provo, Utah 84602, USA. ; Sekhar BB

Subjects: Boron Compounds/Boron Compounds/Boron Compounds/*chemistry ; Glycolates/Glycolates/Glycolates/*chemistry ; Pyrones/Pyrones/Pyrones/*chemistry

  • Source: Organic letters [Org Lett] 2000 Sep 21; Vol. 2 (19), pp. 3035-7.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Selective and unusual fluoride ion complexation by a steroidal receptor using OH...F- and CH...F- interactions: a new motif for anion coordination?

  • Authors : Ghosh S; Department of Organic Chemistry and Solid State and Structural Chemistry Unit, Indian Institute of Science, Bangalore 560 012, India.; Choudhury AR

Subjects: Models, Theoretical*; Chloroform/Chloroform/Chloroform/*chemistry ; Fluorides/Fluorides/Fluorides/*chemistry

  • Source: Organic letters [Org Lett] 2005 Apr 14; Vol. 7 (8), pp. 1441-4.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Enantioselective total synthesis of (+)-rogioloxepane A.

  • Authors : Crimmins MT; Venable and Kenan Laboratories of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA. ; DeBaillie AC

Subjects: Oxepins/Oxepins/Oxepins/*chemical synthesis; Alkadienes/Alkadienes/Alkadienes/chemistry ; Alkylation

  • Source: Organic letters [Org Lett] 2003 Aug 21; Vol. 5 (17), pp. 3009-11.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Anti-selective aldol reactions with titanium enolates of N-glycolyloxazolidinethiones.

  • Authors : Crimmins MT; Venable and Kenan Laboratories of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA. ; McDougall PJ

Subjects: Thiones/Thiones/Thiones/*chemistry ; Titanium/Titanium/Titanium/*chemistry; Alcohols/Alcohols/Alcohols/chemistry

  • Source: Organic letters [Org Lett] 2003 Feb 20; Vol. 5 (4), pp. 591-4.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Print ISSN:

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