MECHANISM OF ELIMINATION REACTIONS - E2 REACTIONS OF SUBSTITUTED ALPHA-PHENYLETHYL BROMIDES

被引：23

|

作者：

YOSHIDA, T

YANO, Y

OAE, S

机构：

来源：

TETRAHEDRON | 1971年 / 27卷 / 22期

关键词：

D O I：

10.1016/S0040-4020(01)91699-0

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：5343 / &

相关论文

共 50 条

[31] KINETIC STUDIES OF SOLVOLYSIS .12. QUESTION OF A SINGLE MECHANISM FOR BORDERLINE SN REACTIONS - SOLVOLYSIS OF OPTICALLY ACTIVE ALPHA-PHENYLETHYL CHLORIDE IN AQUEOUS ETHANOL
OKAMOTO, K
UCHIDA, N
SAITO, S
SHINGU, H
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1966, 39 (02) : 307 - +
[32] SOLVOLYTIC ELIMINATION-REACTIONS OF TERTIARY ALPHA-CSNME2-SUBSTITUTED SYSTEMS
CREARY, X
HATOUM, HN
BARTON, A
ALDRIDGE, TE
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (06): : 1887 - 1897
[33] The stereochemistry of solvent-promoted E1cB/E2 reactions of alpha-indenyl substituted ethyl halides
Meng, QS
Thibblin, A
CHEMICAL COMMUNICATIONS, 1996, (03) : 345 - 346
[34] Relative rates of the gas phase SN2 and E2 reactions of alkyl bromides and alkyl iodides
Gronert, S
Fagin, A
Okamoto, K
Pratt, LM
Mogali, S
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2003, 226 : U181 - U181
[35] THEORETICAL-STUDY OF BIMOLECULAR ELIMINATION (E2) REACTIONS - POSSIBILITY OF SYN E2 ELIMINATION IN THE SERIES OF 2-R-2-R'-1-HALOCYCLOPROPANES
ERMOLAEVA, LV
APPOLONOVA, SA
PLEMENKOV, VV
BOLESOV, IG
KONOVALOV, AI
RUSSIAN CHEMICAL BULLETIN, 1995, 44 (04) : 599 - 602
[36] SYNTHESIS AND CONFORMATION OF R-(+)-2-(ALPHA-PHENYLETHYL)BENZOPHENONE
AKO, M
TAKENAKA, S
CHEMISTRY LETTERS, 1979, (06) : 637 - 640
[37] BORDERLINE SOLVOLYTIC REACTIONS - APPEARANCE OF SOLVENT-PROMOTED E2 REACTION IN COMPETITION WITH STEPWISE ELIMINATION AND SUBSTITUTION-REACTIONS
MENG, QS
THIBBLIN, A
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (06) : 1839 - 1840
[38] NEW MECHANISTIC INTERPRETATION OF E2 REACTIONS
CSAPILLA, J
CHIMIA, 1964, 18 (02) : 37 - &
[39] A THEORETICAL ACCOUNT FOR STEREOSELECTIVE E2 REACTIONS
FUKUI, K
FUJIMOTO, H
TETRAHEDRON LETTERS, 1965, (48) : 4303 - &
[40] Carbon isotope effect studies of the mechanism of the hofmann elimination reaction of para-substituted (2-phenylethyl-l-14C)- and (2-phenylethyl-2-14C)trimethylammonium bromides
1600, (113):

← 1 2 3 4 5 →