Basic information Reaction Safety Supplier Related

(R)-DTBM-SEGPHOS

Basic information Reaction Safety Supplier Related

(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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Safety Information

WGK Germany 
3
HS Code 
2932.99.7000
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(R)-DTBM-SEGPHOS Usage And Synthesis

Reaction

  1. Rhodium catalyzed chemo-, regio, and entantioselective [2 + 2 + 2] cycloaddition of alkynes with isocyanates.
  2. With copper, enantioselective cross Aldol-type reaction of acetonitrile.
  3. With copper, enantioselective vinylsilane alkenylation of aldehydes.
  4. Gold carbene mediated stereoselective cyclopropanation of propargyl esters.
  5. With copper, enantioselective 1,2-reduction of ketones, and 1,4-reduction of a α,β-usaturated esters.
  6. With copper, catalytic enantioselective Mannich-type reaction.
  7. Enantioselective fluorination of b β-keto esters, tert-butoxycarbonyl lactones and lactmes with Sodeoka's Pd-aqua complex and a fluorinating reagent.
  8. Rh-catalyzed intramolecular olefin or carbonyl hydroacylation.
  9. Pd-catalyzed γ-arylation of β,γ-unsaturated ketones.
  10. Involved in numerous conjugate alkynylation, and ring-opening alkynylation of azabenzonorbornadienes.
  11. Involved in asymmetric hydroamination of bicyclic alkenes/dienes,13a diamination of conjugated dienes,13b and hydroalkoxylation/hydrosulfenylation of allenes.
The actions in the following figures are corresponding to the above ones in sequence.

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
Email
chenxi.song@runvmat.com
LaaJoo Gold
Tel
021-60702684 18516024827
Email
huang.jiayi@sinocompound.com
J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788
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jkinfo@jkchemical.com
TCI (Shanghai) Development Co., Ltd.
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021-67121386
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Sales-CN@TCIchemicals.com
Beijing HwrkChemical Technology Co., Ltd
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010-89508211 18501085097
Email
sales.bj@hwrkchemical.com