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(2S,3S,5R)-2-((S)-3-Benzyloxy-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

392663-08-0

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392663-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 392663-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,2,6,6 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 392663-08:
(8*3)+(7*9)+(6*2)+(5*6)+(4*6)+(3*3)+(2*0)+(1*8)=170
170 % 10 = 0
So 392663-08-0 is a valid CAS Registry Number.

392663-08-0Relevant academic research and scientific papers

Total synthesis of (+)-azaspiracid-1. An exhibition of the intricacies of complex molecule synthesis

Evans, David A.,Kvaerno, Lisbet,Dunn, Travis B.,Beauchemin, Andre,Raymer, Brian,Mulder, Jason A.,Olhava, Edward J.,Juhl, Martin,Kagechika, Katsuji,Favor, David A.

supporting information; experimental part, p. 16295 - 16309 (2009/05/08)

The synthesis of the marine neurotoxin azaspiracid-1 has been accomplished. The individual fragments were synthesized by catalytic enantioselective processes: A hetero-Diels-Alder reaction to afford the E- and HI-ring fragments, a carbonyl-ene reaction to furnish the CD-ring fragment, and a Mukaiyama aldol reaction to deliver the FG-ring fragment. The subsequent fragment couplings were accomplished by aldol and sulfone anion methodologies. All ketalization events to form the nonacyclic target were accomplished under equilibrating conditions utilizing the imbedded configurations of the molecule to adopt one favored conformation. A final fragment coupling of the anomeric EFGHI-sulfone anion to the ABCD-aldehyde completed the convergent synthesis of (+)-azaspiracid-1.

Total synthesis and structural elucidation of azaspiracid-1. Construction of key building blocks for originally proposed structure

Nicolaou,Pihko, Petri M.,Bernal, Federico,Frederick, Michael O.,Qian, Wenyuan,Uesaka, Noriaki,Diedrichs, Nicole,Hinrichs, Juergen,Koftis, Theocharis V.,Loizidou, Eriketi,Petrovic, Goran,Rodriquez, Manuela,Sarlah, David,Zou, Ning

, p. 2244 - 2257 (2007/10/03)

Syntheses of the three key building blocks (65, 98, and 100) required for the total synthesis of the proposed structure of azaspiracid-1 (1a) are described. Key steps include a TMSOTf-induced ring-closing cascade to form the ABC rings of tetracycle 65, a neodymium-catalyzed internal aminal formation for the construction of intermediate 98, and a Nozaki-Hiyama-Kishi coupling to assemble the required carbon chain of fragment 100. The synthesized fragments, obtained stereoselectively in both their enantiomeric forms, were expected to allow for the construction of all four stereoisomers proposed as possible structures of azaspiracid-1 (1a-d), thus allowing the determination of both the relative and absolute stereochemistry of the natural product.

Synthesis of the ABCD ring system of azaspiracid

Nicolaou,Qian, Wenyuan,Bernal, Federico,Uesaka, Noriaki,Pihko, Petri M.,Hinrichs, Jrgen

, p. 4068 - 4071 (2007/10/03)

Previously attempted spirocyclizations to form the ABCD ring system of azapiracid (1) have proven unsuccessful owing to the anomeric effects that favor the formation of the undesired 13S diastereomer. By the use of a hydrogen bond donor as an auxiliary gr

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