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Formation of Substituted Tetrahydropyrans through Oxetane Ring Opening: Application to the Synthesis of C1–C17 Fragment of Salinomycin
Organic Letters
◽
10.1021/ol403604u
◽
2014
◽
Vol 16
(3)
◽
pp. 836-839
◽
Cited By ~ 36
Author(s):
J. S. Yadav
◽
Vinay K. Singh
◽
P. Srihari
Keyword(s):
Ring Opening
◽
Oxetane Ring
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Related Documents
Cited By
References
ChemInform Abstract: Enantioselective Oxetane Ring Opening with Chloride: Unusual Use of Wet Molecular Sieves for the Controlled Release of HCl.
ChemInform
◽
10.1002/chin.201641027
◽
2016
◽
Vol 47
(41)
◽
Author(s):
Wen Yang
◽
Zhaobin Wang
◽
Jianwei Sun
Keyword(s):
Controlled Release
◽
Molecular Sieves
◽
Ring Opening
◽
Oxetane Ring
Download Full-text
Tandem Suzuki Coupling/Intramolecular Oxetane Ring Opening to Form Polycyclic Ring Systems
Organic Letters
◽
10.1021/acs.orglett.0c01899
◽
2020
◽
Vol 22
(15)
◽
pp. 5828-5832
◽
Cited By ~ 1
Author(s):
Lindsey G. DeRatt
◽
Edward C. Lawson
◽
Kiran Kumar
◽
Soyon S. Hwang
◽
Renee L. DesJarlais
◽
...
Keyword(s):
Ring Opening
◽
Suzuki Coupling
◽
Ring Systems
◽
Oxetane Ring
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ChemInform Abstract: A Selective Intramolecular Transacylation of Taxoids Accompanying with the Oxetane Ring Opening.
ChemInform
◽
10.1002/chin.201234174
◽
2012
◽
Vol 43
(34)
◽
pp. no-no
Author(s):
Feng Gao
◽
Min Yu
◽
Qiao-Hong Chen
◽
Feng-Peng Wang
Keyword(s):
Ring Opening
◽
Oxetane Ring
Download Full-text
Simple Preparation of Diamondoid 1,3-Dienes via Oxetane Ring Opening§
Organic Letters
◽
10.1021/ol070920n
◽
2007
◽
Vol 9
(13)
◽
pp. 2541-2544
◽
Cited By ~ 31
Author(s):
Andrey A. Fokin
◽
Ekaterina D. Butova
◽
Lesya V. Chernish
◽
Natalie A. Fokina
◽
Jeremy E. P. Dahl
◽
...
Keyword(s):
Ring Opening
◽
Simple Preparation
◽
Oxetane Ring
Download Full-text
ChemInform Abstract: MECHANISM AND STEREOCHEMISTRY OF OXETANE REACTIONS. II. HIGH SYN STEREOSELECTIVITY IN THE OXETANE RING OPENING OF 6-PHENYL-7-OXABICYCLO(4.2.0)OCTANE UNDER ACIDIC CONDITIONS. COMPARISON WITH THE ANALOGOUS REACTIONS OF THE CORRESPONDING
Chemischer Informationsdienst
◽
10.1002/chin.197601204
◽
1976
◽
Vol 7
(1)
◽
pp. no-no
Author(s):
A. BALSAMO
◽
P. CROTTI
◽
M. FERRETTI
◽
F. MACCHIA
Keyword(s):
Ring Opening
◽
Acidic Conditions
◽
Oxetane Ring
Download Full-text
A mild catalytic synthesis of 2-oxazolines via oxetane ring-opening: rapid access to a diverse family of natural products
Chemical Science
◽
10.1039/c9sc03843d
◽
2019
◽
Vol 10
(41)
◽
pp. 9586-9590
◽
Cited By ~ 12
Author(s):
Hai Huang
◽
Wen Yang
◽
Zuliang Chen
◽
Zengwei Lai
◽
Jianwei Sun
Keyword(s):
Natural Products
◽
Ring Opening
◽
Catalytic Synthesis
◽
Rapid Access
◽
Oxetane Ring
A new catalytic protocol for the expedient synthesis of oxazolines from oxetanes is developed.
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Mild C–C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with Soft Carbon Nucleophiles
Angewandte Chemie
◽
10.1002/ange.202013062
◽
2020
◽
Author(s):
Hai Huang
◽
Tianyu Zhang
◽
Jianwei Sun
Keyword(s):
Lewis Acid
◽
Ring Opening
◽
Bond Formation
◽
Carbon Nucleophiles
◽
Acid Catalyzed
◽
Soft Carbon
◽
Oxetane Ring
Download Full-text
Construction of five-membered heterocycles by intramolecular oxetane ring opening
10.14711/thesis-991012662567203412
◽
2018
◽
Author(s):
Renwei Zhang
Keyword(s):
Ring Opening
◽
Oxetane Ring
Download Full-text
1-(Trifluoromethyl)vinylation via Oxirane or Oxetane Ring-Opening: A Facile Synthesis of 4- or 5-Hydroxy-Functionalized 2-Trifluoromethyl-1-alkenes
Synthesis
◽
10.1055/s-2005-918413
◽
2006
◽
Vol 2006
(01)
◽
pp. 128-132
◽
Cited By ~ 1
Author(s):
Junji Ichikawa
◽
Ryo Nadano
Keyword(s):
Ring Opening
◽
Facile Synthesis
◽
Oxetane Ring
Download Full-text
Mild C–C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with Soft Carbon Nucleophiles
Angewandte Chemie International Edition
◽
10.1002/anie.202013062
◽
2020
◽
Author(s):
Hai Huang
◽
Tianyu Zhang
◽
Jianwei Sun
Keyword(s):
Lewis Acid
◽
Ring Opening
◽
Bond Formation
◽
Carbon Nucleophiles
◽
Acid Catalyzed
◽
Soft Carbon
◽
Oxetane Ring
Download Full-text
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