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D-Ring Intermediate

7 The Eschenmoser Synthesis ofA-Ring Intermediate 24 and D-Ring Intermediate 25 [Pg.123]


Both groups wisely elected to couple their ABC-O-D ring intermediates with preformed protected-tripepetides, thus making the synthesis more convergent. As a result, the East and West US-Coast teams entered the end-game with similar intermediates, ie compounds 2 and 3, respectively. [Pg.301]

Nicolaou s total synthesis of the enediyne antibiotic, calicheamicin 71 [19], (Scheme 12.15 to Scheme 12.19) involves several new aspects in carbohydrate chemistry. The calicheamicin 71 oligosaccharide synthesis began with the construction of the D-ring intermediate from L-rhamnose. Thus, L-rhamnose 112 was converted into the glycosyl donor, trichloroacetimidate 118, through the... [Pg.600]

Enamide and enamine photocyclizations (9, 13, 14, 113) are central to yet another strategy which has been successfully employed by Ninomiya (9, 13, 14, 61-71), Kametani (74), and Atta-ur-Rahman (72, 73) in the synthesis of yohimbine alkaloids. These approaches typically begin with harmalane (336) which contains the ABC unit of the pentacyclic yohimbine targets (Scheme 3.56). Condensation of harmalane with an appropriately substituted cyclohexene carboxylic acid or benzoyl chloride 337 affords seco D-ring intermediate 338. To effect D-ring closure, the enamide chromophore in 338 is photocyclized to form pentacyclic enamide 339. Alternatively, photoreaction... [Pg.265]

The a d-selective addition is not always observed in some cases the. -addition product predominates, and sometimes there is no selectivity observed at all. Obviously not all substrates are likely to react via a four-membered ring intermediate like 9. [Pg.233]

Schemes 15 and 16 summarize the syntheses of intermediates that represent rings A and D of vitamin Bi2 by the Eschenmoser group. Treatment of lactam/lactone 51, the precursor to B-ring intermediate 8 (whose synthesis has already been described, see Scheme 8), with potassium cyanide in methanol induces cleavage of the y-lac-tone ring and furnishes intermediate 76 after esterification of the newly formed acetic acid chain with diazomethane. Intermediate 76 is produced as a mixture of diastereomers, epimeric at the newly formed stereocenter, in a yield exceeding 95%. Selective conversion of the lactam carbonyl in 76 into the corresponding thiolactam... Schemes 15 and 16 summarize the syntheses of intermediates that represent rings A and D of vitamin Bi2 by the Eschenmoser group. Treatment of lactam/lactone 51, the precursor to B-ring intermediate 8 (whose synthesis has already been described, see Scheme 8), with potassium cyanide in methanol induces cleavage of the y-lac-tone ring and furnishes intermediate 76 after esterification of the newly formed acetic acid chain with diazomethane. Intermediate 76 is produced as a mixture of diastereomers, epimeric at the newly formed stereocenter, in a yield exceeding 95%. Selective conversion of the lactam carbonyl in 76 into the corresponding thiolactam...
The selective reduction of the D-ring olefin in 106 using a partially poisoned catalyst (Pd/C, 0.25 % pyridine) provided intermediate 107 (83 %), which was epimerized at -78 °C with sodium methoxide (HOAc quench at -78 °C, 89 %) (Scheme 10.9). Deoxygenation by means of tosyl hydrazone 108 and subsequent treatment with catechol borane and tetrabutylammonium acetate gave pentacyclic... [Pg.247]

X. C. Ding, B. F. Rasmussen, G. A. Petsko, D. Ringe, Direct Structural Observation of an Acyl-Enzyme Intermediate in the Hydrolysis of an Ester Substrate by Elastase , Biochemistry 1994, 33, 9285-9293. [Pg.91]


See other pages where D-Ring Intermediate is mentioned: [Pg.124]    [Pg.125]    [Pg.126]    [Pg.536]    [Pg.537]    [Pg.282]    [Pg.288]    [Pg.124]    [Pg.125]    [Pg.126]    [Pg.536]    [Pg.537]    [Pg.282]    [Pg.288]    [Pg.219]    [Pg.436]    [Pg.304]    [Pg.167]    [Pg.127]    [Pg.127]    [Pg.130]    [Pg.459]    [Pg.464]    [Pg.754]    [Pg.760]    [Pg.437]    [Pg.213]    [Pg.230]    [Pg.362]    [Pg.49]    [Pg.75]    [Pg.83]    [Pg.84]    [Pg.96]    [Pg.808]    [Pg.430]    [Pg.89]    [Pg.160]    [Pg.354]    [Pg.439]    [Pg.161]    [Pg.314]    [Pg.186]    [Pg.885]    [Pg.247]    [Pg.578]    [Pg.587]    [Pg.39]   


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