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In principle, each certification authority has to maintain at least two revocation lists: (1) a dated list of the certificates that it has issued and revoked, and (2) a dated list of all the certificates that the authorities know of and recognize as having been revoked The root certification authority and each of its delegate authorities must be able to access these lists to verify the instantaneous state of all the certificates to be treated within the authentication system Revocation can be periodic or exceptional When a certificate expires, the certification authority withdraws it from the directory (but retains a copy in a special directory, to be able to arbitrate any conflict that might arise in the future) Replacement certificates have to be ready and supplied to the owner to ensure the continuity of the service.

or GPL, enforces the goals of the FSF by ensuring that the software can be copied, distributed, modified, and extended, but requires that the software always be free and include source code (which the FSF sees as a condition of software freedom). Applying the GPL is often referred to as copylefting.

The root authority (or one of its delegated authorities) can cancel a certificate before its expiration date, for example, if the certificate owner s private key has been compromised or if there has been any abuse in usage In the case of secure payments, the notion of solvency, ie, that the user has available the necessary funds, is obviously one of the essential considerations The processing of the revocation lists must be speedy to alert users and, in certain countries, the authorities, particularly if the revocation is before the expiration date Perfect synchronization among the various authorities must be attained to avoid questioning the validity of documents signed or encrypted before the withdrawal of the corresponding certificates..

(B.7)

subscriber.setMessageListener( new MessageListener() { public void onMessage( Message message ) { .... } } );

average values for steady-state temperatures when the loss is constant and the temperature is already stabilized at a certain value. The thermal storage capacity should be taken into account to establish the conditions for high time constants during transient and/or heat charge or discharge conditions. Transient-State Thermal Calculations At an instant t < t0 , the external temperature of the reservoir is the lowest temperature, Tlow . At instant t0 , power transference begins, limited by the thermal capacity of the reservoir, which prevents the temperature from rising abruptly (exponentially). To express the instantaneous difference in temperature, it is de ned as T Zth P, where Zth is the reservoir thermal impedance, which varies with time. The equivalent thermal circuit, including the thermal capacity C, is illustrated in Figure 5.3, with its transient response to a sudden power step illustrated in Figure 5.4. The amount of heat Q stored in the

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substituents could be placed on the isopropylidene C-30 methyl group. The 30hydroxy (206) and 30-(hydroxyethyl)thio (197) analogs retained the activity of 187, whereas 30-(diethylaminoethyl)thio (198), aromatic (200), acetamide (202), and 30-pyrrolidine (205) derivatives showed decreased activity. Unlike 197, the 30-(hydroxyethyl) amino analog (203) exhibited dramatically decreased activity. An unsubstituted amino moiety (201) and a free carboxyl (199 and 204) led to complete inactivation. In conclusion, the isopropylidene probably binds to a hydrophobic pocket on the HIV-1 molecular target. A certain lack of steric hindrance accommodates a variety of substituents without improvement of activity. However, amines and carboxylic acid moieties are not favorable (Table 9-8).77 9.4.1.3 Side-Chain Modi cation Elongation of the glycine alkyl chain (one methylene) in 184 to an undecanoic acid in 187 (ten methylenes) resulted in greatly increased activity and a different mechanism of action. This result also suggested that position-28 might accommodate various substituents. Therefore, more compounds were designed to optimize the side chain at this position. First, compounds (207 214, 187, 215, and 216, Figure 9-11) with 1$12 methylenes were synthesized to determine the optimal chain length. These compounds