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

ChemInform Abstract: N-H Insertion Reactions of Rhodium Carbenoids. Part 3. The Development of a Modified Bischler Indole Synthesis and a New Protecting Group Strategy for Indoles.

ChemInform ◽  
2010 ◽  
Vol 33 (47) ◽  
pp. no-no
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: 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

Concise Synthesis of [1,1′-Biisoquinoline]-4,4′-diolviaa Protecting Group Strategy and Its Application for Potential Liquid-Crystalline Compounds

2009 ◽  
Vol 92 (10) ◽  
pp. 2024-2037 ◽  
Author(s):  
Elisabeth Kapatsina ◽  
Markus Mateescu ◽  
Angelika Baro ◽  
Wolfgang Frey ◽  
Sabine Laschat
Keyword(s):  
Liquid Crystalline ◽  
Protecting Group ◽  
Group Strategy

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

Multihydroxy-Functional Polysilanes via an Acetal Protecting Group Strategy

2010 ◽  
Vol 43 (20) ◽  
pp. 8462-8467 ◽  
Author(s):  
Valerie S. Reuss ◽  
Holger Frey
Keyword(s):  
Protecting Group ◽  
Group Strategy

Synthesis of Indole-Dihydroisoquinoline Sulfonyl Ureas via Three-Component Reactions

Synthesis ◽  
2018 ◽  
Vol 50 (24) ◽  
pp. 4963-4981 ◽  
Author(s):  
Stuart Pearson ◽  
Shaun Fillery ◽  
Kristin Goldberg ◽  
Julie Demeritt ◽  
Jonathan Eden ◽  
...  
Keyword(s):  
Protecting Group ◽  
Group Strategy

Isoquinolines activated with sulfamoyl chlorides were reacted with indoles in a 3-component reaction to generate a library of dihydroisoquinoline derivatives. Using a differential protecting group strategy, products could be further derivatised. Synthesis of isoquinoline starting materials using several different methods is also described.

Rhodium(iii)-catalyzed indole synthesis at room temperature using the transient oxidizing directing group strategy

2019 ◽  
Vol 55 (64) ◽  
pp. 9547-9550 ◽  
Author(s):  
Yaping Shang ◽  
Krishna Jonnada ◽  
Subhash Laxman Yedage ◽  
Hua Tu ◽  
Xiaofeng Zhang ◽  
...  
Keyword(s):  
Room Temperature ◽  
Nitroso Group ◽  
Group Strategy ◽  
Internal Alkynes ◽  
Directing Group ◽  
Catalyzed Reactions ◽  
Indole Synthesis

Rh-Catalyzed reactions of N-alkyl anilines with internal alkynes at room temperature have been developed using an in situ generated N-nitroso group as a transient oxidizing directing group.

ChemInform Abstract: A New Protecting Group Strategy for Amino Groups in Oligonucleotide Chemistry: CEOC Group

ChemInform ◽  
2010 ◽  
Vol 30 (43) ◽  
pp. no-no
Author(s):  
Muthiah Manoharan ◽  
Thazha P. Prakash ◽  
Isabelle Barber-Peoc'h ◽  
Balkrishen Bhat ◽  
Guillermo Vasquez ◽  
...  
Keyword(s):  
Protecting Group ◽  
Amino Groups ◽  
Group Strategy
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