Selective tetrafunctionalisation of α-cyclodextrin using the supertrityl protecting group - Synthesis of the first C2-symmetric tetraphosphane based on a cavitand (α-TEPHOS)

European Journal of Organic Chemistry

Volumn , Issue 8, 2003, Pages 1377-1381

  Poorters, Laurent ^a   Armspach, Dominique ^a   Matt, Dominique ^a  

^a UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

Cavitands; Cyclodextrins; Phosphanes

Indexed keywords

6A,6B,6D,6E TETRADEOXY 6A,6B,6D,6E TETRAKIS(DIPHENYLPHOSPHINYL) 2A,2B,2C,2D,2E,3A,3B,3C,3D,3E,3F,6C,6F TETRADECA O METHYL ALPHA CYCLODEXTRIN; ALPHA CYCLODEXTRIN; CARBON; CHLORIDE; REAGENT; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CHEMICAL STRUCTURE; DEPROTECTION REACTION; METHYLATION; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0038709314     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200390193     Document Type: Article

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