Asymmetric synthesis of chiral, Nonracemic dialkyl-α-hydroxyalkylphosphonates via a (−)-Chlorodiiso-pinocampheylborane (Ipc2B-Cl) reduction

[1]  C. Meier,et al.  Asymmetric synthesis of chiral, nonracemic dialkyl-α-, β-, and γ-hydroxyalkylphosphonates via a catalyzed enantioselective catecholborane reduction , 1995 .

[2]  C. Meier,et al.  Synthesis of Protected 3′,5′-Di-2′-Deoxythymidine-(α-hydroxy-2-nitrobenzyl)-phosphonate Diesters as Dimer Building Blocks for Oligonucleotides , 1995 .

[3]  J. Balzarini,et al.  Homo Dinucleoside-α-hydroxyphosphonate Diesters as Prodrugs of the Antiviral Nucleoside Analogues 2′,3′-Dideoxythymidine and 3′-Azido-2′,3′-dideoxythymidine , 1995 .

[4]  F. Hammerschmidt,et al.  Enzymes in organic chemistry, part 2: Lipase-catalysed hydrolysis of 1-acyloxy-2-arylethylphosphonates and synthesis of phosphonic acid analogues of L-phenylalanine and L-tyrosine , 1995 .

[5]  K. Koeller,et al.  Reactions of Chiral Phosphorous Acid Diamides: The Asymmetric Synthesis of Chiral .alpha.-Hydroxy Phosphonamides, Phosphonates, and Phosphonic Acids , 1995 .

[6]  S. Shibuya,et al.  Stereoselective Synthesis of .beta.-Oxygenated .alpha.-Hydroxyphosphonates by Lewis Acid-Mediated Stereoselective Hydrophosphonylation of .alpha.-Benzyloxy Aldehydes. An Application to the Synthesis of Phosphonic Acid Analogs of Oxyamino Acids , 1994 .

[7]  T. Gajda.  Enantioselective synthesis of diethyl 1-hydroxyalkylphosphonates via oxazaborolidine catalyzed borane reduction of diethyl α-ketophosphonates , 1994 .

[8]  K. Koeller,et al.  Asymmetric synthesis of α-hydroxy- phosphonamides, phosphonates and phosphonic acids , 1994 .

[9]  N. Rath,et al.  The enantioselective addition of dialkylphosphites to aldehydes: Catalysis by a lanthanum binaphthoxide complex , 1994 .

[10]  C. Meier.  5′,5′‐O‐Dinucleosid‐α‐hydroxybenzylphosphonsäureester als lipophile, potentielle Prodrugs von 2′,3′‐Didesoxythymidin (ddT) , 1993 .

[11]  T. Yamagishi,et al.  Stereodivergent synthesis of β-amino-α-hydroxyphosphonic acid derivatives by lewis acid mediated stereosclective hydrophosphonylation of α-amino aldehydes , 1993 .

[12]  Michael J. Miller,et al.  EPSP Synthase: The Design and Synthesis of Bisubstrate Inhibitors Incorporating Novel 3-Phosphate Mimics , 1993 .

[13]  P. Ramachandran,et al.  Chiral synthesis via organoboranes. 38. Selective reductions. 48. Asymmetric reduction of trifluoromethyl ketones by B-chlorodiisopinocampheylborane in high enantiomeric purity , 1993 .

[14]  B. Stowasser,et al.  New hybrid transition state analog inhibitors of HIV protease with peripheric C2-symmetry , 1992 .

[15]  Paweł Kafarski,et al.  BIOLOGICAL ACTIVITY OF AMINOPHOSPHONIC ACIDS , 1991 .

[16]  D. Patel,et al.  Preparation of peptidic α-hydroxy phosphonates a new class of transition state analog renin inhibitors , 1990 .

[17]  D. Patel,et al.  Peptidic α-hydroxy phosphinyls C-terminal modification methodology , 1990 .

[18]  P. Ramachandran,et al.  Highly efficient asymmetric reduction of .alpha.-tertiary alkyl ketones with diisopinocampheylchloroborane , 1986 .

[19]  Ab A. Smaardijk,et al.  The absolute configuration of a-hydroxyphosphonates , 1985 .

[20]  H. Wynberg,et al.  Asymmetric catalysis in carbon-phosphorus bond formation , 1984 .

[21]  C. Geiger,et al.  Mesylate derivatives of .alpha.-hydroxy phosphonates. Formation of carbocations adjacent to the diethyl phosphonate group , 1983 .

[22]  K. Berlin,et al.  The Reactions of Aroyl Halides with Phosphites. Esters of Aroylphosphonic Acids , 1964 .