A novel, mild, and facile method to prepare 6-methylidene penem derivatives

被引:13
作者
Abe, T
Sato, C
Ushirogochi, H
Sato, K
Takasaki, T
Isoda, T
Mihira, A
Yamamura, I
Hayashi, K
Kumagai, T
Tamai, S
Shiro, M
Venkatesan, AM
Mansour, TS
机构
[1] Wyeth Lederle Japan Ltd, Med Res Labs, Shiki Shi, Saitama 3538511, Japan
[2] Rigaku Corp, Tokyo 1968666, Japan
[3] Wyeth Ayerst Res, Chem & Screening Sci, Pearl River, NY 10965 USA
关键词
D O I
10.1021/jo049880g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A novel and mild method was established to synthesize 6-methylidene penem compounds. This method entails a MgBr2/Et3N-promoted aldol-type condensation on 6-bromopenem 12 with an appropriately substituted aldehyde to yield the intermediate acetylated bromohydrin, which was smoothly converted to the final product with. simultaneous deprotection of C3 carboxylic acid ester using activated zinc dust and phosphate buffer at pH 6.5. This process provides a useful variation of C-C bond formation method for penem derivatives and also serves as a practical synthetic method to prepare 6-exomethylenepenem derivatives without racemization at the C5 position.
引用
收藏
页码:5850 / 5860
页数:11
相关论文
共 37 条
[1]   Concerning the boron-mediated aldol reaction of carboxylic esters [J].
Abiko, A ;
Liu, JF ;
Masamune, S .
JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (08) :2590-2591
[2]  
AILEEN F, 1981, J ORG CHEM, V46, P2208
[3]  
AOYAGI S, Patent No. 2654076
[4]  
AOYAGI S, 1990, Patent No. 4977256
[5]   6-(SUBSTITUTED METHYLENE)PENEMS, POTENT BROAD-SPECTRUM INHIBITORS OF BACTERIAL BETA-LACTAMASE .3. STRUCTURE-ACTIVITY-RELATIONSHIPS OF THE 5-MEMBERED HETEROCYCLIC-DERIVATIVES [J].
BENNETT, I ;
BROOM, NJP ;
BRUTON, G ;
CALVERT, S ;
CLARKE, BP ;
COLEMAN, K ;
EDMONDSON, R ;
EDWARDS, P ;
JONES, D ;
OSBORNE, NF ;
WALKER, G .
JOURNAL OF ANTIBIOTICS, 1991, 44 (03) :331-337
[6]   6-(SUBSTITUTED METHYLENE)PENEMS, POTENT BROAD-SPECTRUM INHIBITORS OF BACTERIAL BETA-LACTAMASE .5. CHIRAL 1,2,3-TRIAZOLYL DERIVATIVES [J].
BENNETT, IS ;
BROOKS, G ;
BROOM, NJP ;
CALVERT, SH ;
COLEMAN, K ;
FRANCOIS, I .
JOURNAL OF ANTIBIOTICS, 1991, 44 (09) :969-978
[7]   A NEW APPROACH TO THE DIASTEREOSELECTIVE SYNTHESIS OF ALDOLS - INTRODUCTION OF THE 6-ALPHA-(1R-HYDROXYETHYL)SIDE CHAIN OF THE CARBAPENEM AND PENEM ANTIBIOTICS [J].
BOUFFARD, FA ;
SALZMANN, TN .
TETRAHEDRON LETTERS, 1985, 26 (51) :6285-6288
[8]   THIENAMYCIN TOTAL SYNTHESIS .1. SYNTHESIS OF AZETIDINONE PRECURSORS OF (+/-)-THIENAMYCIN AND ITS STEREOISOMERS [J].
BOUFFARD, FA ;
JOHNSTON, DBR ;
CHRISTENSEN, BG .
JOURNAL OF ORGANIC CHEMISTRY, 1980, 45 (06) :1130-1135
[9]  
BROOM NJP, Patent No. 9410178
[10]   PENEM BRL-42715 - AN EFFECTIVE INACTIVATOR FOR BETA-LACTAMASES [J].
BULYCHEV, A ;
MASSOVA, I ;
LERNER, SA ;
MOBASHERY, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (17) :4797-4801