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Mercap tides

DR. BRAUMAN I am glad you asked that question. Mercap-tide ions are frequently pictured in organic chemistry as being incredibly reactive and having unusual properties. However, our experimental results indicate that they fit exactly on the plot which I showed. Thus, in the gas phase, their behavior appears normal. [Pg.106]

Reactive substrates are those with a good leaving group, such as halide (in acyl halides), hydrosulfide (in thioadds), alkyl thiolate or alkyl mercap-tide (in thioesters), and carboxylate (in anhydrides). [Pg.250]

Air sweetening a process in which air or oxygen is used to oxidize lead mercap-tides to disulfides instead of using elemental sulfur. [Pg.416]

Figure 3. Possible route to orbital requirement satisfaction within the organotin mercap-tide series... Figure 3. Possible route to orbital requirement satisfaction within the organotin mercap-tide series...
Caution. The syntheses described below should be carried out in a well-ventilated hood because of the release of CO and the strong stench of mercap-tides. Schlenk-type glassware should be used for most procedures. [Pg.39]

The product obtained in this reaction indicates that terminal mercap-tide groups are much better nucleophiles than bridged groups (34). [Pg.233]

Sulfides. Symmetrical sulfides can be prepared in high yield from the reaction of alkyl halides and sodium sulfide in water with this phase-transfer catalyst. Unsymmetrical sulfides are prepared from alkyl halides and sodium mercap-tides. Secondary alkyl halides react more slowly than primary halides bromides are more reactive than chlorides. ... [Pg.271]

CAS 155-04-4 EINECS/ELINCS 205-840-3 Synonyms 2(3H)-Benzothiazolethione, zinc salt Bis (2-benzothiazolylthio) zinc Bis (mercaptobenzothiazolato) zinc 2-Mercaptobenzothiazole zinc salt Zinc-2-benzothiazolethiolate Zinc benzothiazolyl mercap-tide Zinc benzothiazol-2-ylthiolate Zinc mercaptobenzothiazolate Zinc mercaptobenzothiazolesalt Zinc mercaptobenzylthiazol ZMBT ZnMB Empirical C,4HsN2S4Zn Formula Zn(C,H4NS2)2 Properties M.w. 397.85... [Pg.1424]

Ruf HH, Wende P, Ullrich V (1979) Models for ferric cytochrome P450. Characterization of hemin mercap-tide complexes by electronic and ESR spectra. J Inorg Biochem 11 189-204... [Pg.241]

Newcomers are antimony-based stabilizers. The interest for these compounds is due to the classification, in the United States, of antimony mercap-tide as a nontoxic chemical [39]. [Pg.159]


See other pages where Mercap tides is mentioned: [Pg.604]    [Pg.373]    [Pg.226]    [Pg.604]    [Pg.56]    [Pg.24]    [Pg.57]    [Pg.24]    [Pg.373]    [Pg.373]    [Pg.280]    [Pg.96]    [Pg.618]    [Pg.179]    [Pg.180]    [Pg.391]    [Pg.426]    [Pg.68]    [Pg.100]    [Pg.336]   


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