The Diels-Alder reaction on endohedral Y3N@C78: the importance of the fullerene strain energy.
about
A complete guide on the influence of metal clusters in the Diels-Alder regioselectivity of I(h)-C80 endohedral metallofullerenes.The reactivity of endohedral fullerenes. What can be learnt from computational studies?Chemistry of endohedral metallofullerenes: the role of metals.Current status and future developments of endohedral metallofullerenes.The role of aromaticity in determining the molecular structure and reactivity of (endohedral metallo)fullerenes.Recent progress in the chemistry of endohedral metallofullerenes.Mechanochemistry: one bond at a time.Bingel-Hirsch addition on endohedral metallofullerenes: kinetic versus thermodynamic control.Electrochemical control of the regioselectivity in the exohedral functionalization of C60: the role of aromaticity.Full exploration of the Diels-Alder cycloaddition on metallofullerenes M3N@C80 (M = Sc, Lu, Gd): the D(5h) versus I(h) isomer and the influence of the metal cluster.Evaluation of bonding, electron affinity, and optical properties of M@C28 (M = Zr, Hf, Th, and U): Role of d- and f-orbitals in endohedral fullerenes from relativistic DFT calculations.The Regioselectivity of Bingel-Hirsch Cycloadditions on Isolated Pentagon Rule Endohedral Metallofullerenes.Nucleophilic Substitution (SN 2): Dependence on Nucleophile, Leaving Group, Central Atom, Substituents, and Solvent.Aromaticity as the driving force for the stability of non-IPR endohedral metallofullerene Bingel–Hirsch adductsDiels-Alder and Retro-Diels-Alder Cycloadditions of (1,2,3,4,5-Pentamethyl)cyclopentadiene to La@C2v-C82: Regioselectivity and Product StabilityMaximum Aromaticity as a Guiding Principle for the Most Suitable Hosting Cages in Endohedral MetallofullerenesProduct formation in the Prato reaction on Sc3N@D5h-C80: preference for [5,6]-bonds, and not pyracylenic bondsThe Exohedral Diels-Alder Reactivity of the Titanium Carbide Endohedral Metallofullerene Ti2C2@D3h-C78: Comparison withD3h-C78and M3N@D3h-C78(M=Sc and Y) Reactivity
P2860
Q30667038-ABB25FB8-3671-44B7-8F10-CF79B1FA51BAQ33756358-2861A41D-85DB-46F2-A442-A4DA0E5BCC70Q37857717-BCC56DD9-5212-48F6-8566-42FAD6F87FEFQ38036083-85CE0563-2394-4588-9131-B42B497FD902Q38211982-01E99F10-6B21-4D47-BF15-358063BDB493Q38240159-2BA702DB-C949-4EB2-B7F3-8F8EAD71217AQ41432535-987900AD-E395-43D7-B915-87182ABBA6C9Q42688160-EC372548-0C91-42F5-8C2C-17ED4C47A522Q43405856-D71630B6-796B-4E8D-AE53-6592C0E4051BQ46020143-BD44905E-1CE1-4213-A363-F74B3EF49CD5Q46472477-F5209E1A-94F5-4273-A26F-45F8CC9C4CDFQ48262661-00531CB1-6274-4AD8-A992-06E7138FDDDAQ55280700-DB0EEF54-F428-4CFF-BD5D-0A75D1F115D7Q56880581-61EC32F4-A356-484A-A426-A1ABBD58BFECQ56880585-D671044B-6F12-4B19-A071-98482C82F9ACQ56880592-48DAE3C1-37EA-40CD-8878-5A9C29A55313Q56880605-8307C25F-030F-4472-AECF-F77885463777Q56880608-88B22098-E886-4004-A1A2-DC2E8EB72174
P2860
The Diels-Alder reaction on endohedral Y3N@C78: the importance of the fullerene strain energy.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
The Diels-Alder reaction on en ...... f the fullerene strain energy.
@en
The Diels-Alder reaction on en ...... f the fullerene strain energy.
@nl
type
label
The Diels-Alder reaction on en ...... f the fullerene strain energy.
@en
The Diels-Alder reaction on en ...... f the fullerene strain energy.
@nl
prefLabel
The Diels-Alder reaction on en ...... f the fullerene strain energy.
@en
The Diels-Alder reaction on en ...... f the fullerene strain energy.
@nl
P50
P356
P1476
The Diels-Alder reaction on en ...... f the fullerene strain energy.
@en
P304
P356
10.1021/JA8048783
P407
P577
2009-01-01T00:00:00Z