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Sku SC07-0415_250_MG
US-Strem
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Product Information

Product Name
(5aR,10bS)-(+)-5a,10b-Dihydro-2-(pentafluorophenyl)-4H,6H-indeno2,1-b1,2,4triazolo4,3-d1,4oxazinium tetrafluoroborate, min. 98%
Brand Name
US-Strem
Product Number
07-0415
CAS
872143-57-2
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11547236
IUPAC Name
(1S,9R)-4-(2,3,4,5,6-pentafluorophenyl)-8-oxa-4,5-diaza-2-azoniatetracyclo7.7.0.02,6.011,16hexadeca-2,5,11,13,15-pentaene tetrafluoroborate
InChI Key
CPCMDOOTVHDRTM-CVJFODCESA-N
SMILES
B-(F)(F)(F)F.C1C@@H2C@H(C3=CC=CC=C31)N+4=CN(N=C4CO2)C5=C(C(=C(C(=C5F)F)F)F)F

Description

Technical Notes:
1.Scope of the asymmetric intramolecular Stetter recation catalyzed by chiral nucleophilic triazolinylideneCarbens
2.Catalytic asymmetric Stetter reaction onto vinyl phosphine oxide and vinyl phosphonates .
3.N-Heterocyclic carbene catalyzed asymmetric hydration: Direct synthesis of a-protio and a-deuterio, a chloro and a-fluoro carboxylic acids
4.Chemoselective conversion of a-unbranched aldehydes to amides, esters and carboxylic acids by NHC-catalysis.
5.Extending the Stetter reaction with 1-6 acceptors .
6.N-Heterocyclic carbene-catalyzed/L ewis acid strategy for the stereoselective synthesis of spirocyclic
oxindole -dihydropyranones.
7.Access to P-stereogenic phosphinatesviaN-heterocycle
carbene- catalyzed desymmetrization of bisphenols.
8.N-Heterocyclic carbene catalyzed intramolecular nucleophilic substitution: Enantioselective construction of all carbon quaternary stereocenters.

References Data Source From Pubchem

Using Manganese(IV) Oxide as Oxidant

Publication Name: Science of Synthesis
Publication Date: 2024

Using α-Halo or α-Ring-Fused Aldehydes

Publication Name: Science of Synthesis
Publication Date: 2024

Using Organic Oxidants

Publication Name: Science of Synthesis
Publication Date: 2024