(R)-DTBM-SEGPHOS
(R)-DTBM-SEGPHOS Basic information
- Product Name:
- (R)-DTBM-SEGPHOS
- Synonyms:
-
- (R)-(-)-5,5'-Bis[di(3,5-di-t-butyl-4-methoxyphenyl)phosphino]-4,4'-bi-1,3-benzodioxole,min.98%(R)-DTBM-SEGPHOS
- (R)-DTBM-SEGPHOS(R)
- [(4R)-(4,4μ-bi-1,3-benzodioxole)-5,5μ-diyl]bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphine], (R)-(-)-5,5μ-Bis[di(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-4,4μ-bi-1,3-benzodioxole
- (R)-(-)-5,5'-Bis[di(3,5-di-t-butyl-4-Methoxyphenyl)phosphino]-4,4'-bi-1,3-benzodioxole
- (4R)-[4,4'-Bi-1,3-benzodioxole]-5,5'-diylbis[bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]phosphine
- (R)-()-5,5′-Bis[di(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-4,4′-bi-1,3-benzodioxole
- (R)-DTBM-SEGPHOS
- [(4R)-(4,4′-bi-1,3-benzodioxole)-5,5′-diyl]bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphine]
- CAS:
- 566940-03-2
- MF:
- C74H100O8P2
- MW:
- 1179.55
- Product Categories:
-
- Segphos Series
- Chiral Phosphine
- Mol File:
- 566940-03-2.mol
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(R)-DTBM-SEGPHOS Chemical Properties
- Melting point:
- 126-128°C
- Boiling point:
- 987.3±65.0 °C(Predicted)
- form
- Powder
- color
- off-white
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(R)-DTBM-SEGPHOS Usage And Synthesis
Reaction
- Rhodium catalyzed chemo-, regio, and entantioselective [2 + 2 + 2] cycloaddition of alkynes with isocyanates.
- With copper, enantioselective cross Aldol-type reaction of acetonitrile.
- With copper, enantioselective vinylsilane alkenylation of aldehydes.
- Gold carbene mediated stereoselective cyclopropanation of propargyl esters.
- With copper, enantioselective 1,2-reduction of ketones, and 1,4-reduction of a α,β-usaturated esters.
- With copper, catalytic enantioselective Mannich-type reaction.
- Enantioselective fluorination of b β-keto esters, tert-butoxycarbonyl lactones and lactmes with Sodeoka's Pd-aqua complex and a fluorinating reagent.
- Rh-catalyzed intramolecular olefin or carbonyl hydroacylation.
- Pd-catalyzed γ-arylation of β,γ-unsaturated ketones.
- Involved in numerous conjugate alkynylation, and ring-opening alkynylation of azabenzonorbornadienes.
- Involved in asymmetric hydroamination of bicyclic alkenes/dienes,13a diamination of conjugated dienes,13b and hydroalkoxylation/hydrosulfenylation of allenes.
Uses
Catalyst involved in:
- [3,3]-Sigmatropic rearrangements using cyclopropane probes
- Asymmetric intramolecular hydroacylation of ketoaldehydes
Reactant involved in:
- The synthesis of gold-diphosphine complexes for use as catalysts
- Cycloaddition of allenenes to yield alkylidenecyclobutanes
(R)-DTBM-SEGPHOSSupplier
Xinxiang Runyu Material Co., Ltd. Gold
- Tel
- 166-166-37336996 15690792173
- chenxi.song@runvmat.com
LaaJoo Gold
- Tel
- 021-60702684 18516024827
- huang.jiayi@sinocompound.com
J & K SCIENTIFIC LTD.
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
TCI (Shanghai) Development Co., Ltd.
- Tel
- 021-67121386
- Sales-CN@TCIchemicals.com
Beijing HwrkChemical Technology Co., Ltd
- Tel
- 010-89508211 18501085097
- sales.bj@hwrkchemical.com
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- (S)-(-)-5,5'-Bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole,min.98%(S)-SEGPHOS
- (S)-(+)-5,5'-Bis[di(3,5-di-t-butyl-4-methoxyphenyl)phosphino]-4,4'-bi-1,3-benzodioxole,min.98%(S)-DTBM-SEGPHOS