The stereoselective synthesis of α-substituted β-amino secondary alcohols based on the proline-mediated, asymmetric, three-component Mannich reaction and its application to the formal total synthesis of nikkomycins B and Bx

Tetrahedron

Volumn 61, Issue 48, 2005, Pages 11393-11404

  Hayashi, Yujiro ^a   Urushima, Tatsuya ^a   Shin, Makoto ^a   Shoji, Mitsuru ^a  

^a TOKYO UNIVERSITY OF SCIENCE   (Japan)

Author keywords

Asymmetric synthesis; Mannich reaction; Nikkomycin; Proline; Three component reaction

Indexed keywords

ALCOHOL DERIVATIVE; ALDEHYDE; BETA AMINO ACID; CATECHOL DERIVATIVE; KETONE; LITHIUM DERIVATIVE; NIKKOMYCIN; NIKKOMYCIN B; NIKKOMYCIN B X; PROLINE; UNCLASSIFIED DRUG;

ADDITION REACTION; AMINO TERMINAL SEQUENCE; ARTICLE; MANNICH REACTION; OXIDATION; PRIORITY JOURNAL; REACTION ANALYSIS; REDUCTION; STEREOCHEMISTRY;

EID: 27444446480     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.09.013     Document Type: Article

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