Diastereoselectivity in the O-H Insertion Reactions of Rhodium Carbenoids Derived from Phenyldiazoacetates of Chiral Alcohols. Preparation of .alpha.-Hydroxy and .alpha.-Alkoxy Esters

1995 ◽  
Vol 60 (14) ◽  
pp. 4449-4460 ◽  
Author(s):  
Enrique Aller ◽  
David S. Brown ◽  
Geoffrey G. Cox ◽  
David J. Miller ◽  
Christopher J. Moody
Keyword(s):  
Chiral Alcohols ◽  
Insertion Reactions ◽  
Rhodium Carbenoids

ChemInform Abstract: First Example of Regiospecific Intermolecular C-H Insertion Reactions of Cyclic Rhodium Carbenoids: Novel Synthesis of 3-Indol-3′-yloxindoles.

ChemInform ◽  
2010 ◽  
Vol 33 (34) ◽  
pp. no-no
Author(s):  
Sengodagounder Muthusamy ◽  
Chidambaram Gunanathan ◽  
Srinivasarao Arulananda Babu ◽  
Eringathodi Suresh ◽  
Parthasarathi Dastidar
Keyword(s):  
Insertion Reactions ◽  
Rhodium Carbenoids ◽  
Novel Synthesis

ChemInform Abstract: N-H Insertion Reactions of Rhodium Carbenoids. Part 1. Preparation of . alpha.-Amino Acid and α-Aminophosphonic Acid Derivatives.

ChemInform ◽  
2010 ◽  
Vol 28 (21) ◽  
pp. no-no
Author(s):  
E. ALLER ◽  
R. T. BUCK ◽  
M. J. DRYSDALE ◽  
L. FERRIS ◽  
D. HAIGH ◽  
...  
Keyword(s):  
Amino Acid ◽  
Insertion Reactions ◽  
Aminophosphonic Acid ◽  
Rhodium Carbenoids ◽  
Alpha Amino Acid

N-H Insertion Reactions of Rhodium Carbenoids: A Modified Bischler Indole Synthesis

Synlett ◽  
1998 ◽  
Vol 1998 (2) ◽  
pp. 135-136 ◽  
Author(s):  
Christopher J. Moody ◽  
Elizabeth Swann
Keyword(s):  
Insertion Reactions ◽  
Rhodium Carbenoids ◽  
Indole Synthesis

Diastereoselectivity in the O - H Insertion Reactions of Carbenoids Derived from Phenyldiazoacetates of Chiral Alcohols. II. Comparison of Rhodium(II)- and Acid-Mediated Reactions

1999 ◽  
Vol 52 (2) ◽  
pp. 97 ◽  
Author(s):  
David J. Miller ◽  
Christopher J. Moody ◽  
C. Neil Morffitt
Keyword(s):  
Chiral Alcohols ◽  
Insertion Reactions

Rhodium(II)- or acid-mediated decomposition of 2-diazo-2-phenylacetates of chiral alcohols in the presence of various hydroxylic compounds (ROH) results in the diastereoselective formation of 2- hydroxy-, 2-alkoxy- or 2-trialkylsiloxy-2-phenylacetates, with the acid-mediated process giving the higher diastereoselectivity.

N–H Insertion reactions of rhodium carbenoids. Part 3.1 The development of a modified Bischler indole synthesis and a new protecting-group strategy for indoles

2002 ◽  
pp. 1672-1687 ◽  
Author(s):  
Katherine E. Bashford ◽  
Anthony L. Cooper ◽  
Peter D. Kane ◽  
Christopher J. Moody ◽  
Sendogagounder Muthusamy ◽  
...  
Keyword(s):  
Protecting Group ◽  
Insertion Reactions ◽  
Group Strategy ◽  
Rhodium Carbenoids ◽  
Indole Synthesis

N–H Insertion reactions of rhodium carbenoids. Part 5: A convenient route to 1,3-azoles

Tetrahedron ◽  
2004 ◽  
Vol 60 (18) ◽  
pp. 3967-3977 ◽  
Author(s):  
James R Davies ◽  
Peter D Kane ◽  
Christopher J Moody
Keyword(s):  
Insertion Reactions ◽  
Rhodium Carbenoids ◽  
Convenient Route
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