Studies on the stereocontrolled transformation of nitrohexofuranoses into 2-oxabicyclo[2.2.1]heptanes. V: Synthesis of enantiopure methyl (1R,2R,4S)-2-amino-4-hydroxycyclopentanecarboxylate

Tetrahedron Asymmetry

Volumn 21, Issue 1, 2010, Pages 116-122

  Estévez, Amalia ^a   Soengas, Raquel G ^b   Tato, Rubén ^a   Thomas, Pablo ^a   Estévez, Juan Carlos ^a   Estévez, Ramón J ^a   Sussman, Fredy ^a  

^a UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

^b UNIVERSITY OF A CORUÑA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

2 OXABICYCLO[2.2.1]HEPTANE DERIVATIVE; CYCLOPENTYLAMINE; METHYL 2 AMINO 4 HYDROXYCYCLOPENTANECARBOXYLATE; NATURAL PRODUCT; NITROHEXOFURANOSE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; CALCULATION; CONFORMATION; CYCLIZATION; MOLECULAR MECHANICS; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 76049101324     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.12.018     Document Type: Article

References (20)

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