The single-reference coupled-cluster method has proven very effective in the ab initio description of atomic and molecular systems, but its successful application is limited to states dominated by a single Slater determinant, which is used as the reference. In cases where several determinants are important in the wave function expansion, i.e., we have to deal with nondynamic correlation effects, a multi-reference version of the coupled-cluster method is required. The multi-reference coupled-cluster approaches are based on the effective Hamiltonian formulation providing a two-step procedure, in which dynamic correlation effects can be efficiently evaluated by the wave operator, while nondynamic correlation contributions are given by diagonalization of the effective Hamiltonian in the final step. There are two classical multi-reference coupled-cluster formulations. In this paper, the focus is on the so-called Fock-space coupled-cluster method in its basic version with one- and two-particle operators in the exponent. Computational schemes using this truncation of the cluster operator have been successfully applied in calculations in one- and two-valence sectors of the Fock space. In this paper, we show that the approach can be easily extended and effectively employed in the three-valence sector calculations.