67175-80-8

Upstream product

• 702-23-8 2-(4-Methoxyphenyl)ethanol 
• 7439-93-2 lithium 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 127826-15-7 acetic acid 2-(4-methoxy-cyclohexa-1,4-dienyl)-ethyl ester 
• 32863-02-8 2-(4-oxocyclohexyl)ethyl acetate 
• 628731-60-2 4-(2-(benzyloxy)ethyl)cyclohexan-1-one 
• 1616766-79-0 (R)-2-(4-oxocyclohex-2-en-1-yl)ethyl 4-chlorobenzoate 

Relevant academic research and scientific papers

Synthesis of cationic 1-substituted-dicarbonyl(η5-4- methoxycyclohexadienyl)-(triphenylphosphine)iron complexes

Cationic 1-substituted-dicarbonyl(π5-4-methoxycyclohexadienyl)- (triphenylphosphine)iron complexes 10 form a new class of highly functionalised iron complexes which have never been described. They were obtained from neutral 1-substituted (πsup

First synthesis and reactivity of phosphinite and phosphine bridge chelate dicarbonyl (η5-4-methoxycyclohexadienyl)iron complexes

Chelated dicarbonyl (η4-4-methoxycyclohexadiene) iron complexes 6 and 15 which possess a phosphinite and a phosphine bridge respectively form a new class of iron complexes. Their cations 5 and 16 reacted regioselectively with nucleophiles in go

Reductive cyclization strategy for construction of the highly oxygenated CD ring system of aconitine

The synthesis of a CD ring analogue of aconitine is described. The SmI2-mediated reductive cyclization of an α,β-epoxyketone with a pendant formyl group allowed for stereocontrolled construction of the bicyclo[3.2.1]octane framework. Further ox

Development of an efficient route toward meiogynin A-inspired dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteins

The synthesis, on a large scale, with very good yield and er via an efficient strategy, of a chiral 4-substituted 2-cyclohexenone intermediate, was a milestone in the synthesis of seven analogues of meiogynin A, a natural sesquiterpenoid dimer. These comp

From meiogynin A to the synthesis of dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteins

The synthesis of one of the most potent dual inhibitors of the anti-apoptotic proteins Bcl-xL and Mcl-1 is reported. This analogue of a natural sesquiterpenoid dimer meiogynin A was elaborated by a convergent asymmetric synthesis with 36% yield in ten steps. the Partner Organisations 2014.

γ-turn peptidomimetics as fibrinogen antagonists

This invention relates to a method of inhibiting platelet aggregation, and compounds which are mimics of the peptide sequence Arg-Gly-Asp.

A novel constrained reduced-amide inhibitor of HIV-1 protease derived from the sequential incorporation of γ-turn mimetics into a model substrate

C7 mimetics, designed to lock three amino acid residues of a peptide chain into a γ-turn conformation, were introduced sequentially between the P3 to P2' positions of a model HIV-1 protease substrate I (resulting in compou