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Highly enantioselective synthesis of γ-, δ-, and ε-chiral 1..:

Xu, Shiqing ; Oda, Akimichi ; Kamada, Hirofumi.
Proceedings of the National Academy of Sciences of the United States of America. 111 (2014) 23 - p. 8368-8373 , 2014

Link: https://www.jstor.org/stable/23776425

RT Journal
T1 <Title>Highly enantioselective synthesis of γ-, δ-, and ε-chiral 1-alkanols viaZr-catalyzed asymmetric carboalumination of alkenes (ZACA)–Cu- or Pd-catalyzedcross-coupling</Title>

UL https://suche.suub.uni-bremen.de/peid=jstor-23776425&Exemplar=1&LAN=DE
				
A1 Xu, Shiqing
A1 Oda, Akimichi
A1 Kamada, Hirofumi
A1 Negishi, Ei-ichi
PB National Academy of Sciences
YR 2014
SN 0027-8424
SN 1091-6490
K1 Physical sciences
K1 Chemistry
K1 Chemical compounds
K1 Functional groups
K1 Hydroxyls
K1 Alcohols
K1 Chemicals
K1 Acids
K1 Carboxylic acids
K1 Esters
K1 Chemical reactions
K1 Functional group transfer
K1 Acetylation
K1 Physics
K1 Mechanics
K1 Oscillation
K1 Resonance
K1 Magnetic resonance
K1 Nuclear magnetic resonance
K1 Carbon compounds
K1 Hydrocarbons
K1 Aliphatic hydrocarbons
K1 Alkenes
K1 Reagents
K1 Halogen compounds
K1 Iodides
K1 Mathematics
K1 Pure mathematics
K1 Geometry
K1 Geometric shapes
K1 Polytopes
K1 Polyhedrons
K1 Tetrahedrons
K1 Mathematical physics
K1 Symmetry
K1 Asymmetry
K1 Chirality
K1 Chemical mixtures
K1 Chemical solutions
K1 Solvents
JF Proceedings of the National Academy of Sciences of the United States of America
VO 111
IS 23
SP 8368
OP 8373
LK http://dx.doi.org/https://www.jstor.org/stable/23776425
DO https://www.jstor.org/stable/23776425
SF ELIB - SuUB Bremen

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