@article{xiao_chiral_2014,
	title = {Chiral phosphines in nucleophilic organocatalysis},
	volume = {10},
	copyright = {http://creativecommons.org/licenses/by/2.0},
	issn = {1860-5397},
	url = {https://www.beilstein-journals.org/bjoc/articles/10/218},
	doi = {10.3762/bjoc.10.218},
	abstract = {This review discusses the tertiary phosphines possessing various chiral skeletons that have been used in asymmetric nucleophilic organocatalytic reactions, including annulations of allenes, alkynes, and Morita–Baylis–Hillman (MBH) acetates, carbonates, and ketenes with activated alkenes and imines, allylic substitutions of MBH acetates and carbonates, Michael additions, γ-umpolung additions, and acylations of alcohols.},
	language = {en},
	urldate = {2024-10-25},
	journal = {Beilstein Journal of Organic Chemistry},
	author = {Xiao, Yumei and Sun, Zhanhu and Guo, Hongchao and Kwon, Ohyun},
	month = sep,
	year = {2014},
	pages = {2089--2121},
}

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