New carbon-hydrogen bond activation reaction. Stereospecific abstraction of vinylic protons from rhenium alkene complexes [(η5-C5H5)Re(NO)(PPh3)(H2C=CHR)]+ BF4- by the base t-BuO-K+

被引：0

作者：

机构：

来源：

Peng, Tang-Sheng | 1600年 / 09期

关键词：

Carbon-Hydrogen Bond Activation Reaction - Rhenium Alkene Complexes - Vinylic Deprotonation - Vinylic Proton Abstraction;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

共 50 条

[1] A NEW CARBON HYDROGEN-BOND ACTIVATION REACTION - STEREOSPECIFIC ABSTRACTION OF VINYLIC PROTONS FROM RHENIUM ALKENE COMPLEXES [(ETA-5-C5H5)RE(NO)(PPH3)(H2C=CHR)]+BF4-BY THE BASE TERT-BUO-K+
PENG, TS
GLADYSZ, JA
ORGANOMETALLICS, 1990, 9 (11) : 2884 - 2886
[2] A NEW, STEREOSPECIFIC ALKENE METALATION REACTION - FACILE VINYLIC CARBON-HYDROGEN BOND ACTIVATION IN CHIRAL RHENIUM COMPLEXES [(ETA-5-C5H5)RE(NO)(PPH3)(H2C=CHR)]+BF4-
PENG, TS
GLADYSZ, JA
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1992, 203 : 168 - ORGN
[3] A NEW ALKENE CARBON-HYDROGEN BOND ACTIVATION REACTION - FACILE AND STEREOSPECIFIC VINYLIC DEPROTONATION OF THE CHIRAL CATIONIC RHENIUM ALKENE COMPLEXES [(ETA(5)-C5H5)RE(NO)(PPH(3))(H2C=CHR)](BF4-)
PENG, TS
GLADYSZ, JA
ORGANOMETALLICS, 1995, 14 (02) : 898 - 911
[4] MECHANISM OF EQUILIBRATION OF DIASTEREOMERIC CHIRAL RHENIUM ALKENE COMPLEXES[(ETA-5-C5H5)RE(NO)-(PPH3)(H2C=CHR)]+BF4- - THE METAL TRAVERSES BETWEEN ALKENE ENANTIOFACES WITHOUT DISSOCIATION
PENG, TS
GLADYSZ, JA
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1992, 203 : 167 - ORGN
[5] Mechanism of equilibration of diastereomeric chiral rhenium alkene complexes of the formula [(η5-C5H5)Re(NO)(PPh3)(H2C = CHR)]+BF4-. The metal traverses between alkene enantiofaces without dissociation
1600, (114):
[6] REGIOSPECIFIC, DIASTEREOSPECIFIC AND ENANTIOSPECIFIC NUCLEOPHILIC ADDITIONS TO CHIRAL MONOSUBSTITUTED ALKENE COMPLEXES OF THE FORMULA [ETA-5-C5H5)RE(NO)(PPH3)(H2C=CHR)]+ BF4-
PENG, TS
GLADYSZ, JA
TETRAHEDRON LETTERS, 1990, 31 (31) : 4417 - 4420
[7] MECHANISM OF EQUILIBRATION OF DIASTEREOMERIC CHIRAL RHENIUM ALKENE COMPLEXES OF THE FORMULA [(ETA-5-C5H5)RE(NO)(PPH3)(H2C=CHR)]+BF4- - THE METAL TRAVERSES BETWEEN ALKENE ENANTIOFACES WITHOUT DISSOCIATION
PENG, TS
GLADYSZ, JA
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (11) : 4174 - 4181
[8] SYNTHESIS, STRUCTURE, AND REACTIVITY OF CHIRAL RHENIUM ALKENE COMPLEXES OF THE FORMULA [(ETA-5-C5H5)RE(NO)(PPH3)(H2C=CHR)]+X-
BODNER, GS
PENG, TS
ARIF, AM
GLADYSZ, JA
ORGANOMETALLICS, 1990, 9 (04) : 1191 - 1205
[9] ISOMERIZATION OF DIASTEREOISOMERIC ALKENE COMPLEXES OF THE FORMULA [(ETA-5-C5H5)RE(NO)(PPH3)(H2C=CHR)]+ - THE ALKENE ENANTIOFACE BOUND TO THE METAL CAN FLIP WITHOUT ALKENE DISSOCIATION
PENG, TS
GLADYSZ, JA
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1990, (13) : 902 - 903
[10] AN IMPROVED FUNCTIONAL EQUIVALENT OF THE CHIRAL LEWIS ACID [(ETA-5-C5H5)RE(NO)(PPH3)]+BF4- - GENERATION OF A CHLOROBENZENE ADDUCT AND ITS FACILE CONVERSION TO ALKYNE AND CYCLIC ALKENE COMPLEXES [(ETA-5-C5H5)RE(NO)(PPH3)(L)]+BF4-
KOWALCZYK, JJ
GLADYSZ, JA
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1990, 199 : 278 - INOR

← 1 2 3 4 5 →