A STEREOSELECTIVE CONSTRUCTION OF THE ADJACENT TERTIARY AND QUATERNARY CARBONS BY THE MICHAEL ADDITION

被引:13
作者
YAMAGUCHI, M
HAMADA, M
NAKASHIMA, H
MINAMI, T
机构
关键词
D O I
10.1016/S0040-4039(00)95421-2
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
引用
收藏
页码:1785 / 1786
页数:2
相关论文
共 4 条
[1]  
IWATA C, 1982, CHEM PHARM BULL, V30, P2738
[2]   5-MEMBERED RING SPIRO-ANNULATION VIA THERMAL REARRANGEMENT OF ENOL SILYL ETHERS OF 2-(CYCLOPROPYLMETHYLENE)CYCLOALKANONES - A FORMAL TOTAL SYNTHESIS OF SOME SPIROVETIVANE-TYPE SESQUITERPENOIDS [J].
PIERS, E ;
LAU, CK ;
NAGAKURA, I .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1983, 61 (02) :288-297
[3]   A RATIONALE OF DIASTEREOFACIAL SELECTION IN THE ALKYLATION OF ENDOCYCLIC ENOLATES WITH CHIRALITY AT THE BETA-POSITION [J].
TOMIOKA, K ;
YASUDA, K ;
KAWASAKI, H ;
KOGA, K .
TETRAHEDRON LETTERS, 1986, 27 (28) :3247-3250
[4]   A REGIOSELECTIVE AND STEREOSELECTIVE MICHAEL ADDITION OF AMIDE DIENOLATES TO ALPHA,BETA-UNSATURATED ESTERS [J].
YAMAGUCHI, M ;
HAMADA, M ;
KAWASAKI, S ;
MINAMI, T .
CHEMISTRY LETTERS, 1986, (07) :1085-1088