Diastereoselective catalytic asymmetric nitroaldol reaction utilizing rare earth-Li-(R)-BINOL complex. A highly efficient synthesis of norstatine

Tetrahedron Letters

Volumn 35, Issue 33, 1994, Pages 6123-6126

  Sasai, Hiroaki ^a   Kim, Won Sup ^a   Suzuki, Takeyuki ^a   Shibasaki, Masakatsu ^a   Mitsuda, Masaru ^b   Hasegawa, Junzo ^b   Ohashi, Takehisa ^b  

^a UNIVERSITY OF TOKYO   (Japan)

^b KANEKA CORPORATION   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

3 AMINO 2 HYDROXY 4 PHENYLBUTYRIC ACID; ANTIVIRUS AGENT; KNI 227; KYNOSTATIN 272; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; DRUG SYNTHESIS; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0027993912     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(94)88093-X     Document Type: Article

References (22)

1. Basic character of rare earth metal alkoxides. Utilization in catalytic carbon-carbon bond-forming reactions and catalytic asymmetric nitroaldol reactions
2. Stereoselection in the synthesis of threo- and erythro-3-amino-2-hydroxy-4-phenyl-butanoic acid using chiral acetal templates
3. Tributyltin Cyanide, a Novel Reagent for the Stereoselective Preparation of 3-Amino-2-hydroxy Acids via Cyanohydrin Intermediates
4. An Efficient Synthesis of Optically Active α-(t-Butoxycarbonylamino)-aldehydes from α-Amino Acids