A Telluride-Triggered Nucleophilic Ring Opening of Monoactivated Cyclopropanes1

2004 ◽  
Vol 6 (13) ◽  
pp. 2225-2228 ◽  
Author(s):  
Dmitry V. Avilov ◽  
Mahesh G. Malusare ◽  
Engin Arslancan ◽  
Donald C. Dittmer
Keyword(s):  
Ring Opening ◽  
Nucleophilic Ring Opening

scholarly journals Synthesis of 3,3-Diaryl/Heteroarylpropylamines via Nucleophilic Ring Opening of Activated Azetidines with Arenes and Heteroarenes: New Synthetic Route to (±)Tolterodine

ACS Omega ◽  
2018 ◽  
Vol 3 (12) ◽  
pp. 17562-17572 ◽  
Author(s):  
Gaurav Goswami ◽  
Navya Chauhan ◽  
Abhijit Mal ◽  
Subhomoy Das ◽  
Mowpriya Das ◽  
...  
Keyword(s):  
Ring Opening ◽  
Synthetic Route ◽  
Nucleophilic Ring Opening

scholarly journals (1R,4S,5S)-5-((3-Hydroxypropyl)amino)-4-((1-Methyl-1H-tetrazol-5-yl)thio)Cyclopent-2-en-1-ol

Molbank ◽  
10.3390/m1199 ◽  
2021 ◽  
Vol 2021 (2) ◽  
pp. M1199
Author(s):  
Milene A. G. Fortunato ◽  
Filipa Siopa ◽  
Carlos A. M. Afonso
Keyword(s):  
Spectral Data ◽  
13C Nmr ◽  
Ring Opening ◽  
Environmentally Friendly ◽  
Mass Spectral Data ◽  
Mass Spectral ◽  
Excellent Yield ◽  
Ring Opening Reaction ◽  
Nucleophilic Ring Opening

Using environmentally friendly conditions, the nucleophilic ring-opening reaction of 6-azabicyclo[3.1.0]hex-3-en-2-ol with 1-methyl-1H-tetrazole-5-thiol provided a novel thiol-incorporated aminocyclopentitol, (1R,4S,5S)-5-((3-hydroxypropyl)amino)-4-((1-methyl-1H-tetrazol-5-yl)thio)cyclopent-2-en-1-ol, in excellent yield (95%). The newly synthesized compound was analyzed and characterized via 1H, 13C-NMR, HSQC, and mass spectral data.

ChemInform Abstract: SYNTHESIS AND NUCLEOPHILIC RING-OPENING REACTIONS OF ACTIVATED BICYCLO(3.1.0)HEXANES

1977 ◽  
Vol 8 (10) ◽  
pp. no-no
Author(s):  
K. KONDO ◽  
E. HIRO ◽  
D. TUNEMOTO
Keyword(s):  
Ring Opening ◽  
Ring Opening Reactions ◽  
Nucleophilic Ring Opening

Stereochemistry of the nucleophilic ring-opening of activated bicyclo-[3.1.0]Hexanes.

1977 ◽  
Vol 18 (1) ◽  
pp. 109-112 ◽  
Author(s):  
Daiei Tunemoto ◽  
Nobuhiko Araki ◽  
Kiyosi Kondo
Keyword(s):  
Ring Opening ◽  
Nucleophilic Ring Opening

Synthesis of bioactive indolocarbazoles: synthesis, nucleophilic ring-opening and chiral base desymmetrisation of a cyclic sulfate intermediate

2004 ◽  
Vol 45 (40) ◽  
pp. 7469-7473 ◽  
Author(s):  
Christopher J. Nichols ◽  
Nigel S. Simpkins
Keyword(s):  
Ring Opening ◽  
Nucleophilic Ring Opening

Nucleophilic ring opening of bridging thietane ligands in trirhenium carbonyl cluster complexes

1992 ◽  
Vol 11 (11) ◽  
pp. 3794-3801 ◽  
Author(s):  
Richard D. Adams ◽  
Jeffrey E. Cortopassi ◽  
Stephen B. Falloon
Keyword(s):  
Ring Opening ◽  
Carbonyl Cluster ◽  
Cluster Complexes ◽  
Nucleophilic Ring Opening

ChemInform Abstract: Nucleophilic Ring Opening of 3-Benzyl-1,3-oxazinanes by Reformatsky Reagents. A Synthesis of β-Amino Ester Derivatives.

ChemInform ◽  
2010 ◽  
Vol 22 (22) ◽  
pp. no-no
Author(s):  
A. ALBEROLA ◽  
M. A. ALVAREZ ◽  
C. ANDRES ◽  
A. GONZALEZ ◽  
R. PEDROSA
Keyword(s):  
Ring Opening ◽  
Amino Ester ◽  
Nucleophilic Ring Opening

Origin of regioselectivity in nucleophilic ring-opening reaction of 4-trifluoroacetyl-1,3-oxazolium-5-olates

1998 ◽  
Vol 39 (34) ◽  
pp. 6189-6190 ◽  
Author(s):  
Masami Kawase ◽  
Hiromi Koiwai ◽  
Setsuo Saito ◽  
Teruo Kurihara
Keyword(s):  
Ring Opening ◽  
Ring Opening Reaction ◽  
Nucleophilic Ring Opening
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