GRIGNARD-LIKE ADDITION OF B-ALKENYL-9-BORABICYCLO[3.3.1]NONANES TO ALDEHYDES, A NOVEL SYNTHESIS OF ALLYLIC ALCOHOLS WITH DEFINED STEREOCHEMISTRY

被引：39

作者：

JACOB, P ^{[1
]}

BROWN, HC ^{[1
]}

机构：

[1] PURDUE UNIV,RICHARD B WETHERILL LAB,W LAFAYETTE,IN 47907

来源：

关键词：

D O I：

10.1021/jo00423a050

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：579 / 580

页数：2

共 8 条

[1] Brown, 1972, BORANES ORGANIC CHEM
[2] HYDROBORATION .36. DIRECT ROUTE TO 9-BORABICYCLO[3.3.1]NONANE VIA CYCLIC HYDROBORATION OF 1,5-CYCLOOCTADIENE - 9-BORABICYCLO[3.3.1]NONANE AS A UNIQUELY SELECTIVE REAGENT FOR HYDROBORATION OF OLEFINS
BROWN, HC
KNIGHTS, EF
SCOUTEN, CG
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1974, 96 (25) : 7765 - 7770
[3] BROWN HC, 1975, ORGANIC SYNTHESES VI
[4] BUHLER JD, 1973, THESIS PURDUE U
[5] KRAMER G, IN PRESS
[6] MIKHAILOV BM, 1972, ORGANOMET CHEM REV A, P1
[7] SCOUTEN CG, 1974, THESIS PURDUE U
[8] Silverstein R. M., 1975, SPECTROMETRIC IDENTI