102096-63-9

Upstream product

• 599-04-2 (R)-Pantolacton 
• 79-50-5 (S)-pantolactone 
• 102096-60-6 (R)-4,4-dimethyl-2-oxotetrahydrofuran-3-yl acrylate 
• 78-79-5 isoprene 

Downstream Products

• 102208-60-6 (S)-4-methyl-3-cyclohexene-1-carboxylic acid 
• 1417718-65-0 (S)-5-(3,3-dimethylbut-1-ynyl)-3-(N-isopropyl-4-methylcyclohex-3-enecarboxamido)thiophene-2-carboxylic acid 
• 1417718-78-5 (S)-methyl 5-(3,3-dimethylbut-1-ynyl)-3-(N-isopropyl-4-methylcyclohex-3-enecarboxamido)thiophene-2-carboxylate 
• 141484-05-1 (-)-(1S)-N,4-dimethyl-N-(4-methyl-3-pentenyl)-3-cyclohexenamine 
• 141484-02-8 (-)-(1S)-N,4-dimethyl-3-cyclohexenamine 
• 141484-04-0 (-)-(1S)-N,4-dimethyl-N-(4-methyl-3-cyclohexenyl)-3-pentenamide 
• 1273492-72-0 5-(3,3-dimethyl-but-1-ynyl)-3-[(4-methyl-cyclohex-3-enecarbonyl)-(4-oxo-cyclohexyl)-amino]-thiophene-2-carboxylic acid methyl ester 
• 1273492-66-2 5-(3,3-dimethyl-but-1-ynyl)-3-[(1,4-dioxa-spiro[4.5]dec-8-yl)-(4-methyl-cyclohex-3-enecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester 
• 170080-86-1 (S)-2-methyl-6-keto-(4-methyl-3-cyclohexen-1-yl)-2-hexene 
• 170080-85-0 (S)-4-methyl-3-cyclohexene-1-carbonyl chloride 
• 495-61-4 (S)-1-methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene 

Relevant academic research and scientific papers

Enantioselective total synthesis of sesquiterpenoid phellilane L and its diastereomer

The enantioselective synthesis of phellilane L has been accomplished in six-steps with overall 36% yield. The quinidine-based organocatalytic cyclopropanation of vinyl-ketone with 2-bromo-N,O-dimethylacetamide for the stereoselective construction of subst

Silent catalytic promiscuity in the high-fidelity terpene cyclase δ-cadinene synthase

δ-Cadinene synthase (DCS) is a high-fidelity sesquiterpene synthase that generates δ-cadinene as the sole detectable organic product from its natural substrate (E,E)-FDP. Previous work with this enzyme using substrate analogues revealed the ability of DCS

THIOPHEN-2-CARBOXYLIC ACID DERIVATIVES USEFUL AS INHIBITORS OF FLAVIVIRIDAE VIRUSES

Provided are compounds of Formula I: and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of Flaviviridae virus infections (e.g. hepatitis C infections), particularly drug

INHIBITORS OF FLAVIVIRIDAE VIRUSES

Provided are compounds of Formula I: and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of Flaviviridae virus infections, particularly hepatitis C infections.

INHIBITORS OF FLAVIVIRIDAE VIRUSES

Provided are compounds of Formula I: and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of Flaviviridae virus infections, particularly hepatitis C infections.

Asymmetric synthesis of highly enantiomerically enriched (S)(-)-β-bisabolene

(S)-β-Bisabolene, (S)-1, was synthesized by a synthetic route in which (S)-4-methyl-3-cyclohexene carboxylic acid, (S)-10, which was the key intermediate, was prepared via a highly diastereoselective TiCl4-catalyzed Diels-Alder reaction between

DIASTEREOFACE-DISCRIMINATIVE METAL COORDINATION IN ASYMMETRIC SYNTHESIS: D-PANTOLACETONE AS PRACTICAL CHIRAL AUXILIARY FOR LEWIS ACID CATALYZED DIELS-ALDER REACTIONS

TiCl4-catalyzed Diels-Alder additions of the acrylate of commercial D-pantoloacetone to cyclopentadiene, isoprene and butadiene proceed with very high diastereofacial selectivity.Practical and mechanistic aspects of these reactions are discussed.