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Sku SC15-3712_50_MG
US-Strem
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Product Information

Product Name
(11bR)-4-Hydroxy-2,6-bis(2,4,6-trimethylphenyl)-4-oxide-dinaphtho2,1-d:1',2'-f1,3,2dioxaphosphepin, 98%, (99% ee)
Brand Name
US-Strem
Product Number
15-3712
CAS
695162-87-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11984408
IUPAC Name
13-hydroxy-10,16-bis(2,4,6-trimethylphenyl)-12,14-dioxa-13λ5-phosphapentacyclo13.8.0.02,11.03,8.018,23tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaene 13-oxide
InChI Key
BEHLZZISBCRGSO-UHFFFAOYSA-N
SMILES
CC1=CC(=C(C(=C1)C)C2=CC3=CC=CC=C3C4=C2OP(=O)(OC5=C4C6=CC=CC=C6C=C5C7=C(C=C(C=C7C)C)C)O)C

Application

Technical Notes:
1. Mannich Reaction: Catalyst for the enantioselectively highly-regioselective addition of a silyl dienolate to
imines in good yields to give a,ß-unsaturated õ amino carboxylic esters in one step.
2.Three-component reactions of aldehydes, anilines, and a-isocyanoacetamides in the presence of a catalytic amount of chiral phosphoric acid afforded the 5-(1 -aminoalkyl)-5-a minooxazole
References:
1.Angew. Chem. Int. Ed., 2008, 47, 3631-3634 .
2.Angew. Chem. Int. Ed., 2009, 48, 6717-6721.

References Data Source From Pubchem

Asymmetric Brønsted Acid Catalyzed Cycloadditions of ortho-Quinone Methides and Related Compounds

Publication Name: Synthesis
Publication Date: 2022-04-21
DOI: 10.1055/a-1781-6538

Recent Applications of the Diels–Alder Reaction in the Synthesis of Natural Products (2017–2020)

Publication Name: Synthesis
Publication Date: 2021-08-04
DOI: 10.1055/a-1532-4763

Enantioselective Minisci-Reaction of N-Heterocycles and Amides through Hydrogen-Atom Transfer

Publication Name: Synfacts
Publication Date: 2021-05-18
DOI: 10.1055/s-0040-1706201

Brønsted Acid Catalyzed Vinylogous Mannich Reaction

Publication Name: Synfacts
Publication Date: 2008-07
DOI: 10.1055/s-2008-1077816