Intramolecular 4+3 cycloadditions. Theoretical and experimental evaluation of endo/exo preferences of a cyclopentenyl cation

被引：20

作者：

Cramer, CJ ^{[1
]}

Harmata, M

Rashatasakhon, P

机构：

[1] Univ Missouri, Dept Chem, Columbia, MO 65211 USA

[2] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA

[3] Univ Minnesota, Inst Supercomp, Minneapolis, MN 55455 USA

来源：

JOURNAL OF ORGANIC CHEMISTRY | 2001年 / 66卷 / 16期

关键词：

D O I：

10.1021/jo015695g

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[No abstract available]

引用

页码：5641 / 5644

页数：4

共 17 条

[1]

Cramer CJ, 2000, J PHYS ORG CHEM, V13, P176, DOI 10.1002/(SICI)1099-1395(200003)13:3<176::AID-POC232>3.0.CO

[2]

2-V

[3] Quantum chemical characterization of cycloaddition reactions between the hydroxyallyl cation and dienes of varying nucleophilicity [J].

Cramer, CJ ;

Barrows, SE .

JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (16) :5523-5532

[4]

Frisch M.J., 1998, GAUSSIAN 98

[5] INTRAMOLECULAR 4+3 CYCLOADDITIONS - THE SYNTHESIS OF CYCLOOCTANOIDS [J].

HARMATA, M ;

ELAHMAD, S ;

BARNES, CL .

JOURNAL OF ORGANIC CHEMISTRY, 1994, 59 (06) :1241-1242

[6] Intramolecular 4+3 cycloadditions. Cycloaddition reactions of cyclic alkoxyallylic and oxyallylic cations [J].

Harmata, M ;

Elomari, S ;

Barnes, CL .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (12) :2860-2871

[7]

Hehre W. J., 1986, Ab initio molecular orbital theory

[8]

LI J, 1999, MINNESOTA GAUSSIAN S

[9] Extension of the platform of applicability of the SM5.42R universal solvation model [J].

Li, JB ;

Zhu, TH ;

Hawkins, GD ;

Winget, P ;

Liotard, DA ;

Cramer, CJ ;

Truhlar, DG .

THEORETICAL CHEMISTRY ACCOUNTS, 1999, 103 (01) :9-63

[10] Universal reaction field model based on ab initio Hartree-Fock theory [J].

Li, JB ;

Hawkins, GD ;

Cramer, CJ ;

Truhlar, DG .

CHEMICAL PHYSICS LETTERS, 1998, 288 (2-4) :293-298

← 1 2 →