(11bS)-8,9,10,11,12,13,14,15-Octahydro-4-hydroxy-2,6-bis(triphenylsilyl)-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 98%, (99% ee)|15-0821|1157989-25-7

(11bS)-8,9,10,11,12,13,14,15-Octahydro-4-hydroxy-2,6-bis(triphenylsilyl)-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 98%, (99% ee)

$237.00

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. No lead time available. Please request a quote.
Sku SC15-0821_50_MG
US-Strem
Get Bulk Quote

Product Information

Product Name
(11bS)-8,9,10,11,12,13,14,15-Octahydro-4-hydroxy-2,6-bis(triphenylsilyl)-4-oxide-dinaphtho2,1-d:1',2'-f1,3,2dioxaphosphepin, 98%, (99% ee)
Brand Name
US-Strem
Product Number
15-0821
CAS
1157989-25-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
24873612
IUPAC Name
(13-hydroxy-13-oxo-16-triphenylsilyl-12,14-dioxa-13λ5-phosphapentacyclo13.8.0.02,11.03,8.018,23tricosa-1(23),2,8,10,15,17-hexaen-10-yl)-triphenylsilane
InChI Key
PQNJTMDSQLWCTJ-UHFFFAOYSA-N
SMILES
C1CCC2=C3C4=C5CCCCC5=CC(=C4OP(=O)(OC3=C(C=C2C1)Si(C6=CC=CC=C6)(C7=CC=CC=C7)C8=CC=CC=C8)O)Si(C9=CC=CC=C9)(C1=CC=CC=C1)C1=CC=CC=C1

References Data Source From Pubchem

Enantioselective Syntheses of Yohimbine Alkaloids: Proving Grounds for New Catalytic Transformations
Publication Name: Synthesis
Publication Date: 2022-01-04
DOI: 10.1055/a-1684-2942

Isochromenes Synthesis by Cyclization and Asymmetric Transfer Hydrogenation
Publication Name: Synfacts
Publication Date: 2014-02-17
DOI: 10.1055/s-0033-1340765

Organocatalytic Pictet–Spengler Reaction in Natural Product Synthesis
Publication Name: Synfacts
Publication Date: 2011-11-18
DOI: 10.1055/s-0031-1289376

Synthesis of (R)-Ofloxacin
Publication Name: Synfacts
Publication Date: 2010-11-22
DOI: 10.1055/s-0030-1258872

Brønsted Acid Catalyzed Pictet–Spengler Cyclization of Keto Acids
Publication Name: Synfacts
Publication Date: 2010-11-22
DOI: 10.1055/s-0030-1258929