By JAMES A. RATE and JOHN K . LUEDEMAN of Clemson (I7.S.A.) (Eingegangen am 22. 11. 1979) REES matrix semigroups &I= (S, ,I, -1, P) over a semigroup correspond loosely to the n X n matrix rings over it ring R. It is well known that &(R,)x .=(&(R)),,. Moreover, when S is it finite BRANDT semigroup, S
The Ring of Quotients R[S]: R an Integral Domain and S a Commutative Cancellative Semigroup
✍ Scribed by James A. Bate; John K. Luedeman
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 401 KB
- Volume
- 113
- Category
- Article
- ISSN
- 0025-584X
No coin nor oath required. For personal study only.
✦ Synopsis
The theory of rings of quotients of a given ring has been developed by many authors including Asmo [ l ] , JOHNSON [6], UTUMI [ l l ] , and STENSTEOM [lo]. A corresponding theory of semigroups of quotients has been studied by BERTHUUME [3], MOMORRIS [8], and &KLE [6]. LUEDEMAN [7] has begun the development of a theory of the quotient ring of a semigroup ring R[S]. Using the a-set Z(S) = {J[S]: J E Z and C is a a-set on R } , LUEDEUN has shown that in certain cases &,(,,(R[S]) is a ring isomorphic to Qz(R) [S] where &,,(T) is the UTUMI quotient ring of T over the a-set A. This paper further extends LUEDEMAN'S work by considering the theory of quotient rings of semigroup rings over a a-set Z(A) = { J [ I ] : J € Z, a a-set on R and I € A , a a-set on s}.
I n section 2, conditions under which Z(A) becomes a a-set for R[S] are discussed. In section 3, S is required to be a left Ore monoid with 0 and A consists of left ideals of S containing cancellable elements. Then if R is a ring with identity and Z is a a-set of finite type on R, &L.
(d)(R[S]) is shown to be isomorphic to &(R) [&d(S)].
In section 4, this result is slightly generalized when S is commutative.
📜 SIMILAR VOLUMES
function q : U -+AS with q(u) = a, q(b) = 0, q(c) = c. Then q = a + 0 + c -a0 -ac be + abc = a + c. Corollary 2.9. If K = R a' s a field of chrircccteristl'c 0 and S is nny finite semilcctiice. each element of Qd(S) may be realized i i i IT(&').
## Abstract The oxidation of (‐)‐tabersonine (**1**) with dimethyldioxirane (DMD) in neutral and acidic medium gave 16‐hydroxytabersonine‐__N__‐oxide (**3**) and the didehydrovincamine isomers **4** and **5**, respectively. (+)‐14,15‐Didehydro‐quebrachamine (**7**) furnished the hydroxyindolenine *