Abstract: One aspect of a terminal according to the present disclosure includes a receiving section that receives a plurality of downlink control channels supporting application of different control resource set pool indices, and a control section that, when an offset between at least one of the plurality of downlink control channels and a physical shared channel scheduled by the plurality of downlink control channels is smaller than a given value, controls reception of the physical shared channel, based on a default TCI state configured for each of control resource set pool indices or the default TCI state configured irrespective of control resource set pool indices.

Abstract: A terminal according to an aspect of the present disclosure includes a control section that determines whether two physical downlink control channel (PDCCH) candidates out of a plurality of PDCCH candidates can be allocated, and a receiving section that receives the two PDCCH candidates, when it is determined that the two PDCCH candidates can be allocated. The two PDCCH candidates are present within a same slot or a same span. The two PDCCH candidates are associated with two search space sets. The two PDCCH candidates are linked to each other. When it is determined that the two PDCCH candidates cannot be allocated, the control section determines whether one or more PDCCH candidates out of the plurality of PDCCH candidates can be allocated. According to an aspect of the present disclosure, PDCCH candidates can be appropriately determined.

Abstract: A terminal according to one aspect of the present disclosure includes a receiving section that receives a medium access control-control element (MAC CE) indicating two active transmission configuration indicator (TCI) states for one control resource set, and a control section that, when an information element of a radio link monitoring (RLM) reference signal is not provided, uses a reference signal in at least one TCI state out of the two active TCI states for RLM. According to one aspect of the present disclosure, it is possible to appropriately perform at least one of RLM and BFD.

Abstract: A radio communication node includes: a control unit that a first communication using a first radio link with a lower node and a second communication using a second radio link with a terminal, wherein the control unit: controls the first communication using a first radio resource based on a configuration of a radio resource used in the first radio link, when performing a simultaneous communication of the first communication and the second communication, and performs the first communication using a second radio resource at least including the first radio resource when a condition is satisfied not to perform the simultaneous communication of the first communication and the second communication.

Abstract: A terminal according to one aspect of the present disclosure includes: a control section that determines a downlink control channel (Physical Downlink Control Channel (PDCCH)) to monitor from among PDCCHs in a plurality of control resource sets (CORESETs) overlapping in time, based on a CORESET having two transmission configuration indication states (TCI states) being activated; and a receiving section that monitors the determined PDCCH. According to one aspect of the present disclosure, it is possible to appropriately address collision of a plurality of downlink control channels.

Abstract: A radio communication node 100A acquires, in a case in which a DL transmission timing and a UL transmission timing in a radio communication node 100B, a propagation delay between the radio communication node 100A and the radio communication node 100B and transmits timing information including the propagation delay to the radio communication node 100B.

Abstract: A record of authorization including user information is received and appended to a blockchain. The record of authorization authorizes access by a third-party application to the user information for an access duration. The user information is encrypted by a group key and access duration is based on a change to the group key. The group key comprises a public/private key pair, and the access duration is implemented by an authorization group of nodes having the group key. The group key corresponds to either a valid group key at or near the start of the access duration, that enables decryption of a message in the record of authorization that includes the user information, or an incompatible group key at or after the end of the access duration, that does not enable decryption of the message in the record of authorization that includes the user information.

Abstract: A record of authorization including user information is received and appended to a blockchain. The record of authorization authorizes access by a third-party application to the user information for an access duration. The user information is encrypted by a group key and access duration is based on a change to the group key. The group key comprises a public/private key pair, and the access duration is implemented by an authorization group of nodes having the group key. The group key corresponds to either a valid group key at or near the start of the access duration, that enables decryption of a message in the record of authorization that includes the user information, or an incompatible group key at or after the end of the access duration, that does not enable decryption of the message in the record of authorization that includes the user information.

Abstract: A cyber-physical energy optimization control system for a hybrid electric vehicle includes an information layer which is configured to realize vehicle and road condition information collection, hybrid control unit (HCU) threshold optimization and threshold wireless update loading, and an optimized object plug-in hybrid electric bus (PHEB) as a physical layer.

Abstract: The invention provides a process for production of trans-dibenzoxenopyrrole compounds, in which reduction, leaving group conversion, hydrogenation and methylation are carried out in that order. The process of the invention allows trans-dibenzoxenopyrrole compounds to be produced by a simpler procedure than conventional processes. The invention further provides novel compounds obtained as intermediates in the process, and a process for their production.

Abstract: The present invention provides a process for producing an aromatic unsaturated compound of the formula (4) wherein Ar represents an optionally substituted aromatic group or an optionally substituted heteroaromatic group, and Y represents an electron withdrawing group, which comprises reacting (a) a compound of the formula (1) Ar—H??(1) wherein Ar has the same meaning as defined above with (b) a compound of the formula (2) wherein Y has the same meaning as defined above, and Z represents a lower alkoxy, or a compound of the formula (3) wherein Y and Z have the same meanings as defined above, in the presence of (c) an acid or a compound which generates a mineral acid by its hydrolysis.

Abstract: The invention provides a process for production of trans-dibenzoxenopyrrole compounds, in which reduction, leaving group conversion, hydrogenation and methylation are carried out in that order. The process of the invention allows trans-dibenzoxenopyrrole compounds to be produced by a simpler procedure than conventional processes. The invention further provides novel compounds obtained as intermediates in the process, and a process for their production.

Abstract: The invention provides a process for efficiently producing optically active mirtazapine. Specifically, a process for production of optically active mirtazapine wherein an RS mixture of mirtazapine is optically resolved with optically active tartaric acid in the presence of a solvent. More specifically, a process for production of optically active mirtazapine, characterized by making an RS mixture of mirtazapine contact with optically active tartaric acid in the presence of a solvent, and preferentially crystallizing the optically active mirtazapine salt. The solvent is preferably a mixed solvent consisting of a water-soluble organic solvent and water, and more preferably a mixed solvent consisting of a C1-3 alcohol and water.

Abstract: The present invention provides a process for producing an aromatic unsaturated compound of the formula (4) wherein Ar represents an optionally substituted aromatic group or an optionally substituted heteroaromatic group, and Y represents an electron withdrawing group, which comprises reacting (a) a compound of the formula (1) Ar—H??(1) wherein Ar has the same meaning as defined above with (b) a compound of the formula (2) wherein Y has the same meaning as defined above, and Z represents a lower alkoxy, or a compound of the formula (3) wherein Y and Z have the same meanings as defined above, in the presence of (c) an acid or a compound which generates a mineral acid by its hydrolysis.

Abstract: The present invention provides a process for producing an aromatic unsaturated compound of the formula (4) wherein Ar represents an optionally substituted aromatic group or an optionally substituted heteroaromatic group, and Y represents an electron withdrawing group, which comprises reacting (a) a compound of the formula (1) Ar—H??(1) wherein Ar has the same meaning as defined above with (b) a compound of the formula (2) wherein Y has the same meaning as defined above, and Z represents a lower alkoxy, or a compound of the formula (3) wherein Y and Z have the same meanings as defined above, in the presence of (c) an acid or a compound which generates a mineral acid by its hydrolysis.

Abstract: The present invention provides a process for producing an aromatic unsaturated compound of the formula (4) wherein Ar represents an optionally substituted aromatic group or an optionally substituted heteroaromatic group, and Y represents an electron withdrawing group, which comprises reacting (a) a compound of the formula (1) Ar—H??(1) wherein Ar has the same meaning as defined above with (b) a compound of the formula (2) wherein Y has the same meaning as defined above, and Z represents a lower alkoxy, or a compound of the formula (3) wherein Y and Z have the same meanings as defined above, in the presence of (c) an acid or a compound which generates a mineral acid by its hydrolysis.

Abstract: An epoxytriazole derivative (V) useful as an intermediate for anti-fungal agents and an intermediate therefor having high quality can be produced economically and efficiently by the following industrial means. A compound of the following formula (I) is reacted with trimethyloxosulfonium salt and the like in the presence of a base to give compound (II), this compound is converted to compound (IV), and this compound is reacted with 1,2,4-triazole in the presence of a base. wherein Ar is a phenyl group optionally substituted by 1 to 3 halogen atom(s) or trifluoromethyl group, R is a hydrogen atom or lower alkyl group, and X is a leaving group.

Abstract: An epoxytriazole derivative (V) useful as an intermediate for anti-fungal agents and an intermediate therefor having high quality can be produced economically and efficiently by the following industrial means. A compound of the following formula (I) is reacted with trimethyloxosulfonium salt and the like in the presence of a base to give compound (II), this compound is converted to compound (IV), and this compound is reacted with 1,2,4-triazole in the presence of a base. wherein Ar is a phenyl group optionally substituted by 1 to 3 halogen atom(s) or trifluoromethyl group, R is a hydrogen atom or lower alkyl group, and X is a leaving group.

Abstract: An epoxytriazole derivative (V) useful as an intermediate for anti-fungal agents and an intermediate therefor having high quality can be produced economically and efficiently by the following industrial means. A compound of the following formula (I) is reacted with trimethyloxosulfonium salt and the like in the presence of a base to give compound (II), this compound is converted to compound (IV), and this compound is reacted with 1,2,4-triazole in the presence of a base.

Abstract: An epoxytriazole derivative (V) useful as an intermediate for anti-fungal agents and an intermediate therefor having high quality can be produced economically and efficiently by the following industrial means. A compound of the following formula (I) is reacted with trimethyloxosulfonium salt and the like in the presence of a base to give compound (II), this compound is converted to compound (IV), and this compound is reacted with 1,2,4-triazole in the presence of a base.