M39105

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关键词:'M39105'

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Catalytic enantioselective total synthesis of (−)-ar-Tenuifolene

Shaw K, et al.

Tetrahedron Letters, 61(20), 151850-151850 (2020)

An engineered old yellow enzyme that enables efficient synthesis of (4R,6R)-Actinol in a one-pot reduction system.

Shoichiro Horita et al.

Chembiochem : a European journal of chemical biology, 16(3), 440-445 (2015-02-03)

(4R,6R)-Actinol can be stereo-selectively synthesized from ketoisophorone by a two-step conversion using a mixture of two enzymes: Candida macedoniensis old yellow enzyme (CmOYE) and Corynebacterium aquaticum (6R)-levodione reductase. However, (4S)-phorenol, an intermediate, accumulates because of the limited substrate range of

Chemical transformation of 1, 8-cineole: synthesis of seudenone, an insect pheromone

Silvestre AJD, et al.

Industrial Crops and Products, 12(1), 53-56 (2000)

Cyclic α-Acylvinyl Anionic Synthons: A Novel Synthesis of 2-Trimethylsilyl-3-methyl-cyclohexenone by the Wurtz-Fittig Coupling Reaction

Jyothi D and HariPrasad S

Synthetic Communications, 39(5), 875-879 (2009)

Catalytic asymmetric formal total synthesis of (+)-dichroanone and (+)-taiwaniaquinone H

Li L-Q, et al.

Tetrahedron Letters, 55(43), 5960-5962 (2014)

Aldrichimica Acta, 16, 41-41 (1983)

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