Nucleophilic ring opening of cyclic sulphamidites

Tetrahedron: Asymmetry

Volumn 6, Issue 7, 1995, Pages 1667-1674

  Gautun, Hanna S H ^a   Carlsen, Per H J ^a  

^a NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

2 OXAZOLIDINONE DERIVATIVE; AMINE; AMINOALCOHOL; DIAMINE;

ARTICLE; CHIRALITY; DRUG SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0029099084     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/0957-4166(95)00211-7     Document Type: Article

References (27)

1. From Oxazolines to Precursors of Aminoacids
2. Nucleophilic Addition to Cyclic 1,2-Sulfites.
3. Nucleophilic Ring Opening of Cyclic Sulfites -- a Convenient Method for Selective Functionalisation of 1,2-Diols.
4. Synthesis of homochiral amino alcohols, aziridines and diamines via homochiral cyclic sulphites
5. Substitution de sulfites cycliques osidiques par l'ion azoture
6. Stereoselective Synthesis of (S)-Propranolol by the Cyclic Sulfite Route.
7. Synthesis of Optically Pure 4-Hydroxymethyloxazolidinone as Chiral Serinol Synthon from Glycidol.