Metal-catalyzed hydrostannations
Organostannanes are of tremendous synthetic utility as building blocks in organic chemistry
due to the large number of carbon-carbon bond forming reactions these intermediates …
due to the large number of carbon-carbon bond forming reactions these intermediates …
Allylstannanes and vinylstannanes from stannylcupration of C–C multiple bonds. Recent advances and applications in organic synthesis
A Barbero, FJ Pulido - Chemical Society Reviews, 2005 - pubs.rsc.org
The stannylcupration of allenes and alkynes has emerged as a powerful tool for the
synthesis of allyl-and vinylorganostannanes. The regio-and stereoselectivity of this reaction …
synthesis of allyl-and vinylorganostannanes. The regio-and stereoselectivity of this reaction …
Total synthesis of proposed amphidinolide A via a highly selective ring-closing metathesis
RE Maleczka, LR Terrell, F Geng, JS Ward - Organic Letters, 2002 - ACS Publications
Total Synthesis of Proposed Amphidinolide A via a Highly Selective Ring-Closing Metathesis |
Organic Letters ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters …
Organic Letters ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters …
Enantioselective Synthesis of 15-epi-Haterumalide NA Methyl Ester and Revised Structure of Haterumalide NA
H Kigoshi, M Kita, S Ogawa, M Itoh, D Uemura - Organic letters, 2003 - ACS Publications
The enantioselective synthesis of the enantiomer of the haterumalide NA methyl ester, a
cytotoxic macrolide from an Okinawan sponge, was achieved from the threitol derivative in …
cytotoxic macrolide from an Okinawan sponge, was achieved from the threitol derivative in …
Synthesis of ent-Haterumalide NA (ent-Oocydin A) Methyl Ester
Y Gu, BB Snider - Organic letters, 2003 - ACS Publications
Stille coupling of allylic chloride 26 with vinylstannane 4a afforded 65% of 27 with the
requisite skipped diene, vinyl chloride, and allylic oxygen functionality. Yamaguchi …
requisite skipped diene, vinyl chloride, and allylic oxygen functionality. Yamaguchi …
Highly Regioselective and E/Z-Selective Hydroalkylation of Ynone, Ynoate, and Ynamide via Photoredox Mediated Ni/Ir Dual Catalysis
Exclusively α-and highly E/Z-selective hydroalkylation of ynone, ynoate, and ynamide was
achieved via photoredox mediated Ni/Ir dual catalysis with high atom and step economy …
achieved via photoredox mediated Ni/Ir dual catalysis with high atom and step economy …
Palladium-Catalyzed Synthesis of N-Vinyl Pyrroles and Indoles
M Movassaghi, AE Ondrus - The Journal of organic chemistry, 2005 - ACS Publications
A stereospecific palladium-catalyzed N-vinylation of azaheterocycles with vinyl triflates is
described. Cyclic and acyclic vinyl triflates along with nonnucleophilic azaheterocycles were …
described. Cyclic and acyclic vinyl triflates along with nonnucleophilic azaheterocycles were …
A concise asymmetric synthesis of (−)-rasfonin
Y Huang, AJ Minnaard, BL Feringa - Organic & Biomolecular …, 2012 - pubs.rsc.org
A concise asymmetric synthesis of (−)-rasfonin - Organic & Biomolecular Chemistry (RSC
Publishing) DOI:10.1039/C1OB06700A Royal Society of Chemistry ViewáPDFáVersionPreviousáArticleNextáArticle …
Publishing) DOI:10.1039/C1OB06700A Royal Society of Chemistry ViewáPDFáVersionPreviousáArticleNextáArticle …
Nickel-catalyzed reductive arylation of activated alkynes with aryl iodides
SCM Dorn, AK Olsen, RE Kelemen, R Shrestha… - Tetrahedron letters, 2015 - Elsevier
The direct, regioselective, and stereoselective arylation of activated alkynes with aryl iodides
using a nickel catalyst and manganese reductant is described. The reaction conditions are …
using a nickel catalyst and manganese reductant is described. The reaction conditions are …
A Formal [3,3]-Sigmatropic Rearrangement Route to Quaternary α-Vinyl Amino Acids: Use of Allylic N-PMP Trifluoroacetimidates
DB Berkowitz, B Wu, H Li - Organic letters, 2006 - ACS Publications
Pd (II)-mediated rearrangement of allylic N-PMP (p-methoxyphenyl) trifluoroacetimidates
provides the first formal sigmatropic route to quaternary, α-vinylic amino acids, potential …
provides the first formal sigmatropic route to quaternary, α-vinylic amino acids, potential …