Results
1 -
10 of
19
(Click
here to explore results)
- Selection of cost-effective yet chemically diverse pathways from the networks of computer-generated retrosynthetic plans. Tomasz Badowski, Karol Molga, Bartosz A. Grzybowski
, Chem. Sci.
, 2019
, 10
, 4640
- Asymmetric synthesis of trans-4,5-disubstituted γ-butyrolactones involving a key allylboration step. First access to (−)-nicotlactone B and (−)-galbacin. S. Henrion, A. Macé, M. M. Vallejos, T. Roisnel, B. Carboni, J. M. Villalgordo, F. Carreaux
, Org. Biomol. Chem.
, 2018
, 16
, 1672
- Comparison of the volatile profile of vine-shoots and oak chips by headspace-gas chromatography-mass spectrometry (HS-GC-MS). M. Pilar Delgado de la Torre, Feliciano Priego-Capote, María Dolores Luque de Castro
, Anal. Methods
, 2015
, 7
, 1758
- Catalytic enantioselective iodolactonization reactions. Renate Kristianslund, Jørn Eivind Tungen, Trond Vidar Hansen
, Org. Biomol. Chem.
, 2019
, 17
, 3079
- An efficient enantioselective approach to multifunctionalized γ-butyrolactone: concise synthesis of (+)-nephrosteranic acid. Anju Gehlawat, Ranjana Prakash, Satyendra Kumar Pandey
, RSC Adv.
, 2020
, 10
, 19655
- Cognitive apprenticeship as a vehicle for enhancing the understanding and functionalization of organic chemistry knowledge. Katarina Putica, Dragica D. Trivic
, Chem. Educ. Res. Pract.
, 2016
, 17
, 172
- Stereodifferentiation of oak lactone by using multidimensional chromatographic techniques. Rosa M. Martínez, Carmen Barba, Guillermo Santa-María, Marta Herraiz
, Anal. Methods
, 2016
, 8
, 1505
- Recent reports on the synthesis of γ-butenolide, γ-alkylidenebutenolide frameworks, and related natural products. Shrestha Chatterjee, Rajkumar Sahoo, Samik Nanda
, Org. Biomol. Chem.
, 2021
, 19
, 7298
- Asymmetric synthesis of allylic compounds via hydrofunctionalisation and difunctionalisation of dienes, allenes, and alkynes. Guanlin Li, Xiaohong Huo, Xieyang Jiang, Wanbin Zhang
, Chem. Soc. Rev.
, 2020
, 49
, 2060
- Design of fragrant molecules through the incorporation of rough sets into computer-aided molecular design. Kirridharhapany T. Radhakrishnapany, Chee Yan Wong, Fang Khai Tan, Jia Wen Chong, Raymond R. Tan, Kathleen B. Aviso, Jose Isagani B. Janairo, Nishanth G. Chemmangattuvalappil
, Mol. Syst. Des. Eng.
, 2020
, 5
, 1391