NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
Synonyms
|
JandaJel™-triphenylphosphine
|
Copolymer of styrene and divinylbenzene, diphenylphosphinated
|
Diphenylphosphino-polystyrene
|
Polystyrene crosslinked with divinylbenzene, diphenylphosphinated
|
Triphenylphosphine, polymer-bound
|
Triphenylphosphine, polymer-supported, 1.4-2.0 mmol/g on polystyrene
|
JandaJel™-三苯基膦
|
二苯基膦-聚苯乙烯
|
聚苯乙烯交联二乙烯基苯,二苯基磷化
|
苯乙烯-二乙烯基苯共聚物,二苯基磷化
|
聚合物键合型三苯基膦
|
三苯基膦, 聚合物负载, 1.4-2.0 mmol/g于聚苯乙烯
|
|
|
CAS Number
|
|
MDL Number
|
MFCD00148025
|
MFCD03703012
|
|
|
PubChem SID
|
|
PubChem CID
|
|
DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
DETAILS
DETAILS
Sigma Aldrich
Sigma Aldrich -
93094
|
Packaging 5, 25 g in glass bottle |
Sigma Aldrich -
366455
|
Packaging 5, 25, 100 g in glass bottle Preparation Note Used for the preparation of supported precious metal complexes.1 Used to prepare polymer bound ylides for Wittig reactions. It can also be used to convert alcohols or carboxylic acids to the corresponding chlorides under relatively mild conditions in high yield. |
Sigma Aldrich -
533416
|
Packaging 5 g in glass bottle Legal Information JandaJel is a trademark of Sigma-Aldrich Co. LLC |
Sigma Aldrich -
93093
|
Other Notes Polymer-bound triphenylphosphine is used for preparing polymer-bound yields which are highly useful for Wittig reactions; removal of the polymer at the end of the reaction removes all the phosphine oxide.1,2 Packaging 5, 25 g in glass bottle |
Sigma Aldrich -
14664
|
Packaging 5, 25 g in poly bottle |
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Support for nickel, rhenium and rhodium in hydrogenation: J. Am. Chem. Soc., 97, 1742 (1975); dimerization of alkenes: J. Am. Chem. Soc., 97, 341 (1974) and hydroformylation: J. Am. Chem. Soc., 98 5402 (1976). For the halogenation of carboxylic acid and alkanes in carbon tetrachloride: Synthesis, 1093 (1992). Addition of iodine in DMF esterifies primary and secondary alcohols to their respective formate esters: Med. Res. Rev., 19, 97 (1999).
- • For use in the Mitsunobu reaction: Tetrahedron Lett., 8751 (1998), and the Wittig reaction: J. Org. Chem., 48, 326 (1983); J. Chem. Soc. Perkin 1, 2243 (1998).
- Searching...Please wait...
PATENTS
PATENTS
PubChem Patent
Google Patent