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- Rapid formation of complexity in the total synthesis of natural products enabled by oxabicyclo[2.2.1]heptene building blocks. Corinna S. Schindler, Erick M. Carreira
, Chem. Soc. Rev.
, 2009
, 38
, 3222
- A furan Diels–Alder cycloaddition approach to scyphostatin analogues. Calum J. Fraser, Gareth P. Howell, Joseph P. A. Harrity
, Org. Biomol. Chem.
, 2012
, 10
, 9058
- Role of the A
1,3 allylic interaction on the stereochemistry of formation of Schiff's bases derived from bicyclo[2.2.1]hept-5-en-2-one and 7-oxabicyclo[2.2.1]hept-5-en-2-one. Odón Arjona, Araceli Mallo, Cristina Manzano, Joaquín Plumet, Juan Galbis, Carlos Jaime
, J. Chem. Soc., Perkin Trans. 2
, 1988
, 865
- Index pages
, J. Chem. Soc., Perkin Trans. 2
, 1988
, A001
- (1R,3R)-2-Methylene-1,3-dithiolane 1,3-dioxide: a highly reactive and highly selective chiral ketene equivalent in cycloaddition reactions with a broad range of dienes. Varinder K. Aggarwal, Zeynep Gültekin, Richard S. Grainger, Harry Adams, Peter L. Spargo
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 2771
- C-Glycopyranosyl aldehydes: emerging chiral synthons in organic synthesis. Sandeep Kumar, Vinod Khatri, Priyanka Mangla, Rajni Johar Chhatwal, Virinder S. Parmar, Ashok K. Prasad
, RSC Adv.
, 2023
, 13
, 19898
- Radical-mediated rearrangements: past, present, and future. Xinxin Wu, Zhigang Ma, Tingting Feng, Chen Zhu
, Chem. Soc. Rev.
, 2021
, 50
, 11577