![Asymmetric Iodolactonization: An Evolutionary Account - Nolsøe - 2014 - European Journal of Organic Chemistry - Wiley Online Library Asymmetric Iodolactonization: An Evolutionary Account - Nolsøe - 2014 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/84996209-1993-4d74-ad92-045afde54cc3/mscheme4.jpg)
Asymmetric Iodolactonization: An Evolutionary Account - Nolsøe - 2014 - European Journal of Organic Chemistry - Wiley Online Library
![Catalytic enantioselective iodolactonization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB03160F Catalytic enantioselective iodolactonization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB03160F](https://pubs.rsc.org/image/article/2019/OB/c8ob03160f/c8ob03160f-s3_hi-res.gif)
Catalytic enantioselective iodolactonization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB03160F
![Asymmetric Iodolactonization: An Evolutionary Account - Nolsøe - 2014 - European Journal of Organic Chemistry - Wiley Online Library Asymmetric Iodolactonization: An Evolutionary Account - Nolsøe - 2014 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/3b429ae4-456c-4036-a82b-36626c36902b/mscheme37.jpg)
Asymmetric Iodolactonization: An Evolutionary Account - Nolsøe - 2014 - European Journal of Organic Chemistry - Wiley Online Library
![Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins - Chemical Communications (RSC Publishing) DOI:10.1039/C9CC10080F Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins - Chemical Communications (RSC Publishing) DOI:10.1039/C9CC10080F](https://pubs.rsc.org/image/article/2020/CC/c9cc10080f/c9cc10080f-s1_hi-res.gif)
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins - Chemical Communications (RSC Publishing) DOI:10.1039/C9CC10080F
![Catalytic enantioselective iodolactonization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB03160F Catalytic enantioselective iodolactonization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB03160F](https://pubs.rsc.org/image/article/2019/OB/c8ob03160f/c8ob03160f-s24_hi-res.gif)
Catalytic enantioselective iodolactonization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB03160F
![SOLVED:The iodolactonization of unsaturated carboxylic acids to form lactones is valuable method for the gen- eration of stereogenic centers_ Treatment of 3 with iodine and sodium bicarbonate in acetonitrile (CH,CN) generates iodolactone SOLVED:The iodolactonization of unsaturated carboxylic acids to form lactones is valuable method for the gen- eration of stereogenic centers_ Treatment of 3 with iodine and sodium bicarbonate in acetonitrile (CH,CN) generates iodolactone](https://cdn.numerade.com/ask_images/fc3d94e81bef4fcd95794a2f8f8ec9ad.jpg)
SOLVED:The iodolactonization of unsaturated carboxylic acids to form lactones is valuable method for the gen- eration of stereogenic centers_ Treatment of 3 with iodine and sodium bicarbonate in acetonitrile (CH,CN) generates iodolactone
![SOLVED:10.69 Lactones cyclic esters such as compound A, are prepared by halolactonization, an addition reaction t0 an alkene For example , iodolactonization of B foms lactone C, a key intermediate in the SOLVED:10.69 Lactones cyclic esters such as compound A, are prepared by halolactonization, an addition reaction t0 an alkene For example , iodolactonization of B foms lactone C, a key intermediate in the](https://cdn.numerade.com/ask_images/b67c85bc6b074b84ba7c051a54f24141.jpg)
SOLVED:10.69 Lactones cyclic esters such as compound A, are prepared by halolactonization, an addition reaction t0 an alkene For example , iodolactonization of B foms lactone C, a key intermediate in the
![Asymmetric Iodolactonization: An Evolutionary Account - Nolsøe - 2014 - European Journal of Organic Chemistry - Wiley Online Library Asymmetric Iodolactonization: An Evolutionary Account - Nolsøe - 2014 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/00931b09-4d04-4f84-9688-dcbd7495ab73/mscheme7.jpg)
Asymmetric Iodolactonization: An Evolutionary Account - Nolsøe - 2014 - European Journal of Organic Chemistry - Wiley Online Library
![Catalytic enantioselective iodolactonization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB03160F Catalytic enantioselective iodolactonization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB03160F](https://pubs.rsc.org/image/article/2019/OB/c8ob03160f/c8ob03160f-s14_hi-res.gif)