New high yield syntheses of cyclams using the crab-like cyclization reaction

Tetrahedron Letters

Volumn 31, Issue 8, 1990, Pages 1077-1080

  Bradshaw, Jerald S ^a   Krakowiak, Krzysztof E ^a   Izatt, Reed M ^a   Zamecka Krakowiak, Daria J ^a  

^a BRIGHAM YOUNG UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

1,4,8,11 TETRAAZACYCLOTETRADECANE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; METHODOLOGY; NONHUMAN; PRIORITY JOURNAL;

DECAPODA (CRUSTACEA);

EID: 0025099633     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)88730-4     Document Type: Article

References (29)

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2. The Chemistry of 1,4,7-Triazacyclononane and Related Tridentate Macrocyclic Compounds
3. Macrocyclic polyamines with pendent phenol, catechol, hydroquinone, and pyridine group
4. Antibody labelling with functionalised cyclam macrocycles
5. Reactivity of side chain functional groups in macrocyclic Cu2+ complexes
6. Synthesis and X-ray structural characterisation of seven co-ordinate macrocyclic In3+ complexes with relevance to radiopharmaceutical applications
7. Towards tumour targeting with copper-radiolabelled macrocycle?antibody conjugates
8. Implementation of macrocycle conjugated antibodies for tumour-targetting
9. Enrichment of Amino and Carboxylic Acids Using Copper-loaded Silica Pre-columns Coupled On-line with HPLC
10. Metal Complexes with Macrocyclic Ligands. Part XXVI. Synthesis and spectral properties of Cu2+ complexes with mono-N-functionalized 1,4,8-trimethyl-1,4,8,11-tetraazacyclotetradecanes
11. Metal Complexes with Macrocyclic Ligands, XVIII. A study of steric effects in the Co2+-, Ni2+- and Cu2+-complexes with 1-(2-aminoethyl)- and 1-(2-dimethylaminoethyl)-4,8,11-trimethyl-1,4,8,11-tetraazacyclotetradecane
12. Cu2+-promoted Hydrolysis of cyanomethyl-substituted tetra-azamacrocycles
13. Synthesis of an optically active C-funtiopnalized cyclam: (S)-5-(hydroxymethyl)-1,4,8,11-tetra-azacyclotetradecane and itws nickel(II) complex
14. Flow synthesis. Substitute for the high-dilution steps in cryptate synthesis