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C ring

In the case of the aspidosperma structure, the 5-mcmbcrcd C-ring is constructed from the A -acyl substituent. For the kopsine skeleton, an allyl group is installed and used to form the C6-C20 bridge. [Pg.168]

This ring closure is the final step of the reaction of hydrazines with 1,3-difunctional compounds (Section 4.04.3.1.2(ii)), and numerous examples in the literature of pyrazoles have been described. In some cases the N—C ring closure occurs by a concerted mechanism, classified by Huisgen (80AG(E)947) as 1,5-electrocyclizations. [Pg.275]

FIG. 28-18 Specimens for stress-corrosion tests, (a) Bent beam, (h) C ring, (c) U Lend, (d) Tensile, (e) Tensile, (f) Tensile, (g) Notched C ring, (h) Notched tensile. ( ) Precracked, wedge open-loading type. (/) Precracked, cantilever beam. [Chem. Eng., 78, 159 (Sept. 20 1971).]... [Pg.2436]

Part 1 (Volume 1) deals with (a) the nomenclature and the literature of heterocyclic compounds (Chapters 1.02 and 1.03), (b) various special topics (Chapters 1.04-1.15), and (c) rings containing less common heteroatoms (Chapters 1.16-1.22). [Pg.1]

Figure 6-23. Schematic cf an c-ring suppcrted squeeze film damper. Figure 6-23. Schematic cf an c-ring suppcrted squeeze film damper.
Caustic, 50% Misco C Misco C 18-8 Misco C Ring Misco C Carbon Steel Misco C... [Pg.110]

Sulfuric Acid, Below 55% Hard Rubber Lined C.l. Special Rubber Carbon Steel Hastelloy C Ring Packing Special Rubber Special Rubber... [Pg.111]

Iodine azide, on the other hand, forms pure adducts with A -, A - and A -steroids by a mechanism analogous to that proposed for iodine isocyanate additions. Reduction of such adducts can lead to aziridines. However, most reducing agents effect elimination of the elements of iodine azide from the /mwj -diaxial adducts of the A - and A -olefins rather than reduction of the azide function to the iodo amine. Thus, this sequence appears to be of little value for the synthesis of A-, B- or C-ring aziridines. It is worthy to note that based on experience with nonsteroidal systems the application of electrophilic reducing agents such as diborane or lithium aluminum hydride-aluminum chloride may yet prove effective for the desired reduction. Lithium aluminum hydride accomplishes aziridine formation from the A -adducts, Le., 16 -azido-17a-iodoandrostanes (97) in a one-step reaction. The scope of this addition has been considerably enhanced by the recent... [Pg.24]

In a special case involving a C-ring aza steroid, it was found that epoxida-tion of a A -20-keto grouping using a two-phase system (t-butyl alcohol-aqueous potassium hydroxide-30 % hydrogen peroxide) was much superior to the standard hydrogen peroxide-aqueous methanolic alkali conditions. [Pg.196]

D Rotor of stainless steel transmission wheel (e), c-ring ), fixed metal sleeve g), three-way stop-cock (/j), clamps (/). [Pg.291]

The reduction of 2-methyl-1,2,3,4-tetrahydro-y-carboline (92) with zinc and hydrochloric acid in the presence of mercuric chloride gives the indolenine derivative, 2-methyl-l,2,3,4,4a,9b-hexahydro-y-carbo-line (93). A related compound, 4,9b-diethyl-2-methyl-l,2,3,4,4a,9b-hexahydro-y-carboline (96), was obtained by catalytic hydrogenation of 95, which was prepared by Fischer ring closure of the phenyl-hydrazone 94. The stereochemistry of the B/C ring junction in these... [Pg.107]

In a six-step synthesis of (5)-camptothecin (20010L4255), the final step involved a C-ring closure using the Heck reaction. As shown in Scheme 17, 2-chloroquinoline 146 was treated with 15% (PPh3)2Pd(OAc)2 and two equivalents KOAc in CH3CN at 100 °C, affording (5)-campotothecin (147) in 64% yield. [Pg.24]

The dehydration reaction leads by an Ea process to 8 and is promoted by the tertiary, benzylic nature of the OH group at Ce and its antiperiplanar trans relationship to the H atom at Csg. Furthermore, one of the cannonical forms of the enolizable 0-dicarbonyl system present at Cn and Cia has a double bond in the C ring. Thus, dehydration leads to aromatization of the C ring, and this factor must provide some of the driving force for the reaction. [Pg.212]

Caustic, 50% (Max. Temp. 200° F.) Misco C Misco C 18-8 Stainless Steel Misco C Ring Packing... [Pg.211]

Method for the preparation and use of uniaxially loaded tension specimens Method for the preparation and use of C-ring specimens... [Pg.1098]


See other pages where C ring is mentioned: [Pg.134]    [Pg.550]    [Pg.551]    [Pg.425]    [Pg.421]    [Pg.428]    [Pg.438]    [Pg.443]    [Pg.569]    [Pg.220]    [Pg.151]    [Pg.21]    [Pg.397]    [Pg.397]    [Pg.408]    [Pg.190]    [Pg.4]    [Pg.308]    [Pg.102]    [Pg.367]    [Pg.368]    [Pg.724]    [Pg.149]    [Pg.193]    [Pg.127]    [Pg.149]    [Pg.167]    [Pg.188]    [Pg.627]    [Pg.627]    [Pg.627]    [Pg.1383]    [Pg.1388]    [Pg.1388]   
See also in sourсe #XX -- [ Pg.1093 ]




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Analogs with C-methyl (and Other Hydrocarbon) Substituents in the Piperidine Ring

C Ring and Its Substitutions

C ring substitutions

C-Glycosylation of aromatic ring

C-Glycosylation of heterocyclic ring

C-ring specimens

Direct Ring C-H Metallation

Enantioselective Ring Construction by Intramolecular C-H Insertion

Flavonoids, C-ring

Fused ring C-glycoside

Involved in C-Ring Modifications

Modifications at C-5 and Substitution for the Ring Oxygen

New Methods for C-N Ring Construction

Oxygen Function at C-4 of the Piperidine Ring

Ring Compounds with P, Se and C Atoms

Ring Metallation and Reactions of C-Metallated Derivatives

Ring N-C(sp

Ring N-C(sp2)S

Ring Substitution and C-acylations

Ring cleavage via C-deprotonation

Stereoselective C-N Ring Construction

Typical Ring Synthesis of a Pyridine Involving Only C-Heteroatom Bond Formation

Typical Ring Synthesis of a Pyrrole Involving Only C-Heteroatom Bond Formation

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