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Sku SC15-5622_50_MG
US-Strem
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Product Information

Product Name
5-(11bR)-5H-Dibenzb,fazepine-dinaphtho2,1-d:1',2'-f1,3,2dioxaphosphepin-4-yl, 95%
Brand Name
US-Strem
Product Number
15-5622
CAS
1265884-98-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
46844662
IUPAC Name
11-(12,14-dioxa-13-phosphapentacyclo13.8.0.02,11.03,8.018,23tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaen-13-yl)benzob1benzazepine
InChI Key
KOVOHCVLXRKTGN-UHFFFAOYSA-N
SMILES
C1=CC=C2C(=C1)C=CC3=C2C4=C(C=CC5=CC=CC=C54)OP(O3)N6C7=CC=CC=C7C=CC8=CC=CC=C86

Safety Information

Storage Condition
Store at 2-8℃

Application

Technical Notes
1.Ligand for the Ir-catalyzed enantioselective polyene cyclization .
2.Ligand for Ir-catalyzed enantio- and diastereodivergent a allylation of branched and linear aldehydes.
3.Ligand for the direct Ir-catalyzed cross-coupling between branched, racemic allylic alcohols and simple
olefins .
4.Ligand for the Ir-catalyzed enantioselective allyl-allylsilane cross-coupling.
5.Ligand for the Ir or Pd/aminocatalyst-catalyzed and asymmetric v- allylation of a, ß-unsaturated aldehydes.
6.Ligand for the a-allylation of protected a-amino- and a-hydroxyacetaldehydes .
7.Ligand for the Ir-catalyzed substitution of allylic carbonates using formaldehyde N,N-dialkylhydrazones as neutral C1-nucleophiles.
8.Used in synthesis of chiral, ß-substituted homoallylic organoboronic esters via Ag-assisted, Ir- catalyzed allylation of bis(pinacolato )borylmethane.
9.L igand for the Ir-catalyzed enantioselective allylic alkylation that enables the preparation of ß-substituted v,õ- unsaturated esters and protected aldehydes .
10. L igand for the enantioconvergent C(sp3)- -C(sp3) coupling between racemic allenylic electrophiles and
alkylzinc reagents to generate highly asymmetric preparation of allenylic carbonates over the corresponding diene isomers.
11. Ligand used in Pd catalyzed tandem allylation/1 ,2-boronate rearrangement for the asymmetric synthesis of indolines with adjacent quaternary stereocenters .
12. Ligand for the Ir-catalyzed enantioselective allylation of N-, 0- and S-nucleophiles, also chloro- and
Bromoacetaldehyde in water.
13. L igand for the Ir-catalyzed allylic alkylation of racemic allylic alcohols with malonates .
14. L igand for the Ir-catalyzed enantioselective allylation of aryl enamides and enecarbamates .

References Data Source From Pubchem

Synthesis from α,α-Diboryl Carbanions

Publication Name: Science of Synthesis
Publication Date: 2023

Nonstabilized Carbon Nucleophiles

Publication Name: Science of Synthesis
Publication Date: 2023

Enantioselective Addition of 1,3-Diketones to 1,1-Disubstituted Terminal Allenes

Publication Name: Science of Synthesis
Publication Date: 2023

Stereodivergent Dual Catalysis

Publication Name: Science of Synthesis
Publication Date: 2023