(E,E)-10-(1,3-DIHYDRO-4,6-DIHYDROXY-7-METHYL-3-OXOISOBENZOFURAN-5-YL)-4,8-DIMETHYLDECA-4,8-DIENOIC ACID - TOTAL SYNTHESIS AND ROLE IN MYCOPHENOLIC-ACID BIOSYNTHESIS

被引:30
作者
COLOMBO, L
GENNARI, C
POTENZA, D
SCOLASTICO, C
ARAGOZZINI, F
机构
[1] UNIV MILAN,CNR,CTR SOSTANZE ORGAN NAT,IST CHIM ORGAN,I-20133 MILAN,ITALY
[2] UNIV MILAN,FAC AGRARIA,CATTEDRA MICROBIOL IND,I-20133 MILAN,ITALY
关键词
D O I
10.1039/c39790001021
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
引用
收藏
页码:1021 / 1022
页数:2
相关论文
共 13 条
[1]   TOTAL SYNTHESIS OF MYCOPHENOLIC ACID, SOME ANALOGS AND SOME BIOGENETIC INTERMEDIATES [J].
CANONICA, L ;
RINDONE, B ;
SCOLASTICO, C ;
SANTANIELLO, E .
TETRAHEDRON, 1972, 28 (16) :4395-+
[2]   BIOSYNTHESIS OF MYCOPHENOLIC-ACID - OXIDATION OF 6-FARNESYL-5,7-DIHYDROXY-4-METHYLPHTHALIDE IN A CELL-FREE PREPARATION FROM PENICILLIUM-BREVICOMPACTUM [J].
COLOMBO, L ;
GENNARI, C ;
SCOLASTICO, C .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1978, (10) :434-434
[3]  
COREY EJ, 1976, TETRAHEDRON LETT, P809
[4]  
COREY EJ, 1975, TETRAHEDRON LETT, P2647
[5]  
HARRISON IT, 1969, CHEM COMMUN, P616
[6]   A SIMPLE STEREOSELECTIVE VERSION OF CLAISEN REARRANGEMENT LEADING TO TRANS-TRISUBSTITUTED OLEFINIC BONDS . SYNTHESIS OF SQUALENE [J].
JOHNSON, WS ;
WERTHEMANN, L ;
BARTLETT, WR ;
BROCKSOM, TJ ;
LI, TT ;
FAULKNER, DJ ;
PETERSEN, MR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1970, 92 (03) :741-+
[7]   PREPARATION AND ANTITUMOR PROPERTIES OF ANALOGS AND DERIVATIVES OF MYCOPHENOLIC ACID [J].
JONES, DF ;
MILLS, SD .
JOURNAL OF MEDICINAL CHEMISTRY, 1971, 14 (04) :305-&
[8]   COMBINED RADIOGAS CHROMATOGRAPH MASS SPECTROMETER DETECTS INTERMEDIATES IN MYCOPHENOLIC ACID BIOSYNTHESIS [J].
NULTON, CP ;
NAWORAL, JD ;
CAMPBELL, IM ;
GROTZINGER, EW .
ANALYTICAL BIOCHEMISTRY, 1976, 75 (01) :219-233
[9]   LABELED ACETONE AND LEVULINIC ACID ARE FORMED WHEN [C-14]ACETATE IS BEING CONVERTED TO MYCOPHENOLIC-ACID IN PENICILLIUM-BREVICOMPACTUM [J].
NULTON, CP ;
CAMPBELL, IM .
CANADIAN JOURNAL OF MICROBIOLOGY, 1978, 24 (02) :199-201
[10]  
Tamelen E. E. V., 1970, J AM CHEM SOC, V92, P2139