Racemic compound against racemic conglomerate formation: The crystal properties of allylbenzylmethylphenylphosphonium iodide as compared with the nitrogen analogue

Chirality

Volumn 21, Issue 7, 2009, Pages 637-641

  Bredikhin, Alexander A ^a   Eliseenkova, Rimma M ^a   Bredikhina, Zemfira A ^a   Dobrynin, Alexey B ^a   Kostyanovsky, Remir G ^b  

^a A E ARBUZOV INSTITUTE OF ORGANIC AND PHYSICAL CHEMISTRY   (Russian Federation)

^b SEMENOV INSTITUTE OF CHEMICAL PHYSICS   (Russian Federation)

Author keywords

Absolute configuration; Ammonium and phosphonium salts; Conformational mobility; Multiple molecule crystallization; Spontaneous resolution; X ray analysis

Indexed keywords

ALLYLBENZYLMETHYLPHENYLPHOSPHONIUM IODIDE; AMMONIUM DERIVATIVE; NITROGEN DERIVATIVE; PHOSPHONIUM DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL BOND; COMPARATIVE STUDY; CONTROLLED STUDY; CRYSTAL STRUCTURE; CRYSTALLIZATION; DIASTEREOISOMER; MELTING POINT; MOLECULAR DYNAMICS; PRIORITY JOURNAL; RACEMIC MIXTURE; SOLID STATE; STEREOCHEMISTRY; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 70349556096     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20660     Document Type: Article

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