A HOMOLOGATION OF ALDEHYDES AND KETONES VIA THE FORMATION AND THE SUBSEQUENT PUMMERER-TYPE RING FISSION OF 2-METHYLSULFINYL-5,6-DIHYDRO-4H-1,3,4-THIADIAZINE DERIVATIVES

被引：3

作者：

SHIMADA, K ^{[1
]}

OTAKI, A ^{[1
]}

YANAKAWA, M ^{[1
]}

MABUCHI, S ^{[1
]}

YAMAKADO, N ^{[1
]}

SHIMOGUCHI, T ^{[1
]}

INOUE, K ^{[1
]}

KAGAWA, T ^{[1
]}

SHOJI, K ^{[1
]}

TAKIKAWA, Y ^{[1
]}

机构：

[1] IWATE UNIV, FAC ENGN, DEPT APPL CHEM & MOLEC SCI, MORIOKA, IWATE 020, JAPAN

来源：

CHEMISTRY LETTERS | 1995年 / 10期

关键词：

D O I：

10.1246/cl.1995.925

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A two-carbon homologation of aldehydes and ketones was achieved by using a sequence involving the formation and the subsequent Pummerer-type ring fission of 5,6-dihydro-4H-1,3,4-thiadiazine rings possessing methylsulfinyl functionality at C-2.

引用

页码：925 / 926

页数：2